TWI655299B - High-strength steel plate and manufacturing method thereof - Google Patents

High-strength steel plate and manufacturing method thereof Download PDF

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TWI655299B
TWI655299B TW107114474A TW107114474A TWI655299B TW I655299 B TWI655299 B TW I655299B TW 107114474 A TW107114474 A TW 107114474A TW 107114474 A TW107114474 A TW 107114474A TW I655299 B TWI655299 B TW I655299B
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steel sheet
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surface layer
strength steel
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TW201842207A (en
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藪翔平
林宏太郎
虻川玄紀
上西朗弘
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日商新日鐵住金股份有限公司
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/01Layered products comprising a layer of metal all layers being exclusively metallic
    • B32B15/011Layered products comprising a layer of metal all layers being exclusively metallic all layers being formed of iron alloys or steels
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0205Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/60Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur

Abstract

本發明提供一種可適用作為汽車零件用胚料之具有彎曲加工性且含有大量Mn之高強度鋼板及其製造方法。一種彎曲性優異之高強度鋼板,包含板厚中心部、與形成於該板厚中心部之單面或雙面的表層軟化部;該彎曲性優異之高強度鋼板之特徵在於:前述板厚中心部之平均Mn濃度大於4.0質量%且小於10.0質量%,各表層軟化部具有板厚之0.1%到30%的厚度,前述表層軟化部之Mn濃度為2.5質量%以下,且前述表層軟化部的再結晶率為90%以上。The present invention provides a high-strength steel sheet having bending workability and containing a large amount of Mn, which can be suitably used as a blank for automobile parts, and a method for manufacturing the same. A high-strength steel sheet with excellent bendability includes a center portion of the plate thickness and a single-sided or double-sided surface layer softening portion formed in the center portion of the plate thickness. The high-strength steel plate with excellent bendability is characterized in that: The average Mn concentration of the surface layer is greater than 4.0% by mass and less than 10.0% by mass. Each surface layer softened portion has a thickness of 0.1% to 30% of the plate thickness. The surface layer softened portion has a Mn concentration of 2.5% by mass or less. The recrystallization rate is 90% or more.

Description

高強度鋼板及其製造方法High-strength steel plate and manufacturing method thereof

本發明係關於一種彎曲性優異之含Mn濃度高之高強度鋼板及其製造方法。The present invention relates to a high-strength steel sheet with high Mn concentration and excellent bending properties, and a method for manufacturing the same.

背景技術 為達成汽車車體及零件等的輕量化與安全性二者,作為該等之胚料的鋼板正持續朝高強度化發展。一般來說,若將鋼板高強度化,延伸率便會降低而損及鋼板的成形性。因此,為了要使用高強度鋼板作為汽車用構件,必須提高相反特性之強度與成形性二者。BACKGROUND ART In order to achieve both weight reduction and safety of automobile bodies and parts, steel sheets used as the raw materials of these materials are continuously being developed with high strength. Generally, if the strength of a steel sheet is increased, the elongation will decrease and the formability of the steel sheet will be impaired. Therefore, in order to use a high-strength steel sheet as an automobile component, it is necessary to improve both the strength and formability of the opposite characteristics.

為了使延伸率提升,截至目前,提案有一種利用殘留沃斯田鐵(殘留γ)的變態誘發塑性之鋼,即所謂的TRIP鋼(例如:專利文獻1)。In order to improve the elongation, a so-called TRIP steel (for example, Patent Document 1) has been proposed as a steel that utilizes the deformation induced plasticity of residual Vostian iron (residual γ).

另外,提案有一種添加有大於4.0%的Mn之鋼,以作為殘留沃斯田鐵量多於上述TRIP鋼且延展性超越上述TRIP鋼之鋼板(例如:非專利文獻1)。由於上述鋼含有大量Mn,因此對使用其之構件的輕量化效果也很顯著。In addition, a steel with more than 4.0% Mn added has been proposed as a steel plate having a residual amount of Vastfield iron greater than the above-mentioned TRIP steel and having ductility exceeding the above-mentioned TRIP steel (for example, Non-Patent Document 1). Since the above-mentioned steel contains a large amount of Mn, the effect of reducing the weight of components using the same is also significant.

然而,上述鋼因含有大量Mn,故凝固時之Mn偏析會明顯化。若在Mn偏析顯著之組織中,會在Mn濃化區形成有硬質組織偏在之帶狀組織。However, since the above-mentioned steel contains a large amount of Mn, Mn segregation at the time of solidification becomes apparent. In a structure with significant Mn segregation, a band-like structure with a hard structure tends to be formed in the Mn-concentrated region.

一般已知一旦有帶狀組織形成,在如彎曲加工這類伴隨有局部變形之成形中,會容易發生變形局部化且該等變形集中部會成為破裂之起點,故成形性會顯著劣化。It is generally known that once a band-like structure is formed, in the forming accompanied by local deformation such as bending, localization of deformation is easy to occur and the deformation concentrated portion becomes the starting point of cracking, so the formability is significantly deteriorated.

因此,為了實現彎曲加工性優異且含有大量Mn的鋼,減低Mn偏析就變得很重要。Therefore, in order to realize a steel having excellent bending workability and containing a large amount of Mn, it is important to reduce Mn segregation.

例如專利文獻2中揭示有一種成形性優異之鋼板,如實施例所示地,其係藉由使用含有麻田散鐵分率為20%以上之鋼板,將冷軋、酸洗後之鋼板暫時加熱至750℃以上的溫度區,使濃化於帶狀組織中之Mn分散,並使帶狀組織之厚度變薄且細微地分散。For example, Patent Document 2 discloses a steel sheet having excellent formability. As shown in the example, it is a method of temporarily heating a cold-rolled and pickled steel sheet by using a steel sheet containing 20% or more of Asada's loose iron fraction. In the temperature range above 750 ° C, the Mn concentrated in the band structure is dispersed, and the thickness of the band structure is thinned and finely dispersed.

然,鋼板之彎曲加工中,會對彎曲外周表層部之圓周方向施加很大的拉伸應力,另一方面會對彎曲內周表層部施加很大的壓縮應力,故表層部狀態會大大影響超高強度冷軋鋼板之彎曲性。However, in the bending process of steel plates, a large tensile stress will be applied to the circumferential direction of the curved outer surface portion, and a large compressive stress will be applied to the curved inner surface portion, so the state of the surface layer will greatly affect the Bendability of high strength cold rolled steel sheet.

於是,建立了以下假設:藉由改善表層之Mn偏析,就可以緩和彎曲加工時產生於鋼板表面的拉伸應力、壓縮應力,並可改善彎曲性。Therefore, the following hypothesis was established: by improving the Mn segregation of the surface layer, the tensile stress and compressive stress generated on the surface of the steel sheet during bending processing can be reduced, and the bendability can be improved.

在此,作為改質表層的手段,可想到利用包層鋼板。Here, as a means for modifying the surface layer, it is conceivable to use a clad steel sheet.

專利文獻3中揭示了一種包層鋼板的製造方法,該包層鋼板可減低翹曲,且係由母材鋼、不鏽鋼、Ni及Ni合金中之一種所構成。Patent Document 3 discloses a method for manufacturing a clad steel sheet, which can reduce warpage and is made of one of a base metal steel, stainless steel, Ni, and an Ni alloy.

並且,作為改質表層的手段,也提案了一種冷噴塗(cold spray)法的利用。專利文獻4中揭示了一種具有含Mn之基板部與Mn濃度低的堆積層(表層)之冷軋鋼板,且前述Mn濃度低的堆積層(表層)係利用冷噴塗法形成於基板部之至少一側。In addition, as a means for modifying the surface layer, the use of a cold spray method has also been proposed. Patent Document 4 discloses a cold-rolled steel sheet having a substrate portion containing Mn and a deposition layer (surface layer) having a low Mn concentration, and the deposition layer (surface layer) having a low Mn concentration is formed on at least the substrate portion by a cold spray method. One side.

發明人等根據上述假設,製作了使表層之平均Mn濃度減得較中心層之平均Mn濃度更低的包層鋼板,並對包層鋼板調查了冷軋、退火後之鋼板的彎曲性。Based on the above assumptions, the inventors have produced a clad steel sheet in which the average Mn concentration in the surface layer is lower than the average Mn concentration in the center layer, and the clad steel sheet has been examined for its bendability after cold rolling and annealing.

又,如專利文獻4之數個實施例所記載,在形成堆積層(表層)前熱軋延平均Mn濃度高之基板部,並藉由冷噴塗法於熱軋延後之基板部上形成平均Mn濃度低的堆積層(表層),且調查了冷軋、退火後之鋼板的彎曲性。又,如專利文獻4之其他實施例所記載,使用平均Mn濃度高之冷軋板作為基板部,並藉由冷噴塗法在冷軋板上形成平均Mn濃度低之堆積層(表層),並且也調查了退火後之鋼板的彎曲性。In addition, as described in several examples of Patent Document 4, a substrate portion having a high average Mn concentration is hot-rolled before forming a build-up layer (surface layer), and an average is formed on the substrate portion after hot-rolling by a cold spray method. The deposited layer (surface layer) having a low Mn concentration was examined for the bendability of the steel sheet after cold rolling and annealing. Further, as described in other examples of Patent Document 4, a cold rolled sheet having a high average Mn concentration is used as a substrate portion, and a cold spray method is used to form a stacked layer (surface layer) having a low average Mn concentration on the cold rolled sheet, and The bendability of the annealed steel sheet was also investigated.

然而,卻發現到即便已緩和了表層之Mn偏析,仍無法改善彎曲性。However, it was found that even if the Mn segregation in the surface layer had been alleviated, the bendability could not be improved.

先前技術文獻 專利文獻 專利文獻1:日本專利特開平5-59429號公報 專利文獻2:日本專利特開2002-88447號公報 專利文獻3:日本專利特開平1-192404號公報 專利文獻4:日本專利特開2015-193892號公報 非專利文獻Prior Art Literature Patent Literature Patent Literature 1: Japanese Patent Laid-Open No. 5-59429 Patent Literature 2: Japanese Patent Laid-Open No. 2002-88447 Patent Literature 3: Japanese Patent Laid-Open No. 1-192404 Patent Literature 4: Japanese Patent Non-Patent Document No. 2015-193892

非專利文獻1 古川敬、松村理著,「已施行單純熱處理之低碳鋼中之殘留沃斯田鐵的形成與機械性質」(“熱處理”,日本熱處理協會,平成9年,第37號卷,第4號),p.204Non-Patent Document 1 Takagawa Furukawa and Matsumura, "Formation and Mechanical Properties of Remaining Vostian Iron in Low-Carbon Steels That Have Been Simply Heat-treated" ("Heat Treatment", Japan Heat Treatment Association, Heisei 9, Vol. 37 , No. 4), p. 204

發明概要 發明欲解決之課題 本發明之目的在於提供一種能可靠地解決上述習知技術存在之問題,且可適用作為汽車零件用胚料之具有彎曲加工性且含有大量Mn之鋼板及其製造方法。SUMMARY OF THE INVENTION Problems to be Solved by the Invention An object of the present invention is to provide a steel sheet having bending workability and containing a large amount of Mn, which is capable of reliably solving the problems existing in the above-mentioned conventional technologies, and which is applicable as a blank for automobile parts and a method for manufacturing the same. .

用以解決課題之手段 本發明人等為解決有關超高強度鋼板之彎曲性的問題,而積極努力進行了檢討。首先,本發明人等調查了即便使用已使表層之平均Mn濃度減得較中心層之平均Mn濃度更低的包層鋼板,但彎曲性仍未改善的主要原因。Means for Solving the Problem The present inventors have actively conducted a review in order to solve the problem of the bendability of an ultra-high-strength steel sheet. First, the present inventors investigated the main reason why the bendability was not improved even when a clad steel sheet having a lower average Mn concentration in the surface layer than in the center layer was used.

其結果,發現到以下情形係彎曲性劣化的主要原因:為了提高含有大量Mn的中心層之延展性,必須將冷軋後之退火溫度設為低溫,但另一方面,在低溫之退火中,表層之再結晶並未充分進行,導致硬質之未再結晶組織成為破裂之起點。As a result, it was found that the main reason for the deterioration of the bendability was: in order to improve the ductility of the center layer containing a large amount of Mn, the annealing temperature after cold rolling must be set to a low temperature, but on the other hand, in the low-temperature annealing, The recrystallization of the surface layer did not proceed sufficiently, resulting in a hard, non-recrystallized structure as a starting point for cracking.

又,本發明人等也針對即便使用了已令冷噴塗法所形成之堆積層(表層)的平均Mn濃度減得較基板部之平均Mn濃度更低的冷軋鋼板,仍無法改善彎曲性的主要原因進行了調查。In addition, the inventors have also pointed out that even if a cold-rolled steel sheet whose average Mn concentration of the build-up layer (surface layer) formed by the cold spraying method is reduced to be lower than the average Mn concentration of the substrate portion is used, the bendability cannot be improved. The main reasons were investigated.

其結果得知:若為在形成堆積層(表層)前熱軋延平均Mn濃度高之基板部後,藉由冷噴塗法在熱軋延後之基板部上形成平均Mn濃度低的堆積層(表層),並行冷軋、退火而製得鋼板的情況,由於堆積層(表層)之再結晶率差,故彎曲性不會提升。As a result, it was found that if a substrate portion having a high average Mn concentration is hot-rolled before forming a build-up layer (surface layer), a cold spray method is used to form a low-average Mn concentration on the substrate portion after hot-rolling ( (Surface layer), in the case of a steel sheet produced by cold rolling and annealing in parallel, the recrystallization rate of the deposited layer (surface layer) is poor, so the bendability will not be improved.

並且得知:當使用平均Mn濃度高之冷軋板作為基板部,並藉由冷噴塗法於冷軋板上形成平均Mn濃度低之堆積層(表層)後,進行退火而製得鋼板時,由於堆積層(表層)中會有氣孔產生,故彎曲性不會提升。此外,也發現到:由於堆積層(表層)之結晶粒徑會粗大化,故無法確保充分之彎曲性。It was also found that when a cold-rolled sheet with a high average Mn concentration was used as the substrate portion, and a cold-sprayed method was used to form a stacked layer (surface layer) with a low average Mn concentration on the cold-rolled sheet, and then annealing was performed to obtain a steel sheet, Since pores are generated in the stacked layer (surface layer), the flexibility is not improved. In addition, it was found that since the crystal grain size of the build-up layer (surface layer) is coarsened, sufficient bendability cannot be secured.

因此,本發明人等進行了更詳細之檢討。其結果得知:將具有某種特徵之鋼板熔接於母材兩面,並以特定條件進行熱軋延及冷軋延而製得冷軋板,藉由以特定條件將該冷軋板退火,便可保持中心層之延展性且最能改善彎曲性。Therefore, the present inventors conducted a more detailed review. As a result, it was found that a steel plate having certain characteristics was welded to both sides of the base material, and hot-rolled and cold-rolled were produced under specific conditions to obtain a cold-rolled plate. By annealing the cold-rolled plate under specific conditions, It can maintain the ductility of the center layer and can best improve the bendability.

該效果之機制被認為係因多層鋼板之表層的Mn濃度減低導致Mn偏析受到抑制,並且已充分再結晶,而致使彎曲表面中之變形的局部化受到抑制,並因表層延展性之提升而抑制了破裂之產生。並且,亦可想到係因表層之再結晶粒徑(肥粒鐵粒徑)變得微細,故彎曲性更加提升。The mechanism of this effect is thought to be that the Mn segregation is suppressed due to the reduction of the Mn concentration in the surface layer of the multilayer steel sheet, and the Mn segregation has been sufficiently recrystallized, so that the localization of deformation in the curved surface is suppressed, and the surface layer ductility is suppressed The rupture occurred. In addition, it is also conceivable that the recrystallized grain size (ferrous grain iron grain size) of the surface layer becomes fine, so that the bendability is further improved.

依所述製得之本發明之要旨如下。 (1)一種高強度鋼板,包含板厚中心部、與 形成於該板厚中心部之單面或雙面的表層軟化部; 該高強度鋼板之特徵在於: 前述板厚中心部之平均Mn濃度大於4.0質量%且小於10.0質量%, 各表層軟化部具有板厚之0.1%到30%的厚度, 前述表層軟化部之平均Mn濃度為2.5質量%以下, 前述表層軟化部之表層的再結晶率為90%以上,且 前述表層軟化部之再結晶組織的平均結晶粒徑為0.1μm以上且40μm以下。 (2)如上述(1)之高強度鋼板,其中前述板厚中心部以質量%計含有: C:大於0.05%且小於0.80%、 Si:0.001%以上且小於3.50%、 Mn:大於4.0%且小於10.0%、 P:0.10%以下、 S:0.010%以下、 sol.Al:0.001%以上且小於3.00%、及 N:小於0.050%,且 剩餘部分由鐵及無法避免之不純物所構成。 (3)如上述(2)之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素: Cr:0.01%以上且2.00%以下、 Mo:0.01%以上且2.00%以下、 Cu:0.01%以上且2.00%以下、及 Ni:0.01%以上且2.00%以下。 (4)如上述(2)或(3)之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素: Ti:0.005%以上且0.30%以下、 Nb:0.005%以上且0.30%以下、 V:0.005%以上且0.30%以下、及 W:0.005%以上且0.30%以下。 (5)如上述(2)至(4)中任一項之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素: B:0.0001%以上且0.010%以下、 Ca:0.0001%以上且0.010%以下、 Mg:0.0001%以上且0.010%以下、 Zr:0.0001%以上且0.010%以下、及 REM:0.0001%以上且0.010%以下。 (6)如上述(2)至(5)中任一項之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素: Sb:0.0005%以上且0.050%以下、 Sn:0.0005%以上且0.050%以下、及 Bi:0.0005%以上且0.050%以下。 (7)如上述(2)至(6)中任一項之高強度鋼板,其中前述表層軟化部之C量係前述板厚中心部之C量的0.9倍以下。 (8)如上述(3)至(7)中任一項之高強度鋼板,其中前述表層軟化部之Cr量及Mo量的總和係前述板厚中心部之Cr量及Mo量的總和的0.9倍以下。 (9)如上述(3)至(8)中任一項之高強度鋼板,其中前述表層軟化部之Cu量及Ni量的總和係前述板厚中心部之Cu量及Ni量的總和的0.9倍以下。 (10)如上述(4)至(9)中任一項之高強度鋼板,其中前述表層軟化部之Ti量及Nb量的總和係前述板厚中心部之Ti量及Nb量的總和的0.9倍以下。 (11)如上述(4)至(10)中任一項之高強度鋼板,其中前述表層軟化部之V量及W量的總和係前述板厚中心部之V量及W量的總和的0.9倍以下。 (12)如上述(5)至(11)中任一項之高強度鋼板,其中前述表層軟化部之B量係前述板厚中心部之B量的0.9倍以下。 (13)如上述(1)至(12)中任一項之高強度鋼板,其於前述表層軟化部表面更包含熔融鍍鋅層、合金化熔融鍍鋅層或電鍍鋅層。 (14)一種高強度鋼板之製造方法,係製造如上述(1)至(13)中任一項之高強度鋼板的方法; 該高強度鋼板之製造方法之特徵在於包含以下步驟: 在構成前述板厚中心部之母材鋼板的單面或雙面上積層構成前述表層軟化部之表層軟化部用鋼板,以形成多層鋼板; 將前述多層鋼板加熱至加熱溫度1080℃以上且1300℃以下,以及在精整軋延開始溫度800℃以上且1000℃以下之條件下進行熱軋延; 在前述精整軋延結束後2秒以內將前述熱軋延後之多層鋼板冷卻至500℃以上且700℃以下; 在將前述多層鋼板冷卻至前述500℃以上且700℃以下之溫度後,保持3秒以上; 將前述在500℃以上且700℃以下之溫度下保持3秒以上後的多層鋼板酸洗,接著以20%以上且70%以下之軋縮率進行冷軋延;及 將前述冷軋延後之多層鋼板在600℃以上且750℃以下之溫度下保持5秒以上,接著進行冷卻。 (15)如上述(14)之高強度鋼板之製造方法,其以600℃以下之捲取溫度來捲取前述在500℃以上且700℃以下之溫度下保持3秒以上後的多層鋼板。 (16)如上述(15)之高強度鋼板之製造方法,其在前述冷軋延前,在300℃以上且550℃以下之溫度下保持前述捲取後之多層鋼板並進行回火。The gist of the present invention obtained as described is as follows. (1) A high-strength steel plate comprising a center portion of the plate thickness and a single-sided or double-sided surface layer softening portion formed in the center portion of the plate thickness; The high-strength steel plate is characterized by: the average Mn concentration in the center portion of the plate thickness More than 4.0% by mass and less than 10.0% by mass, each surface layer softened portion has a thickness of 0.1% to 30% of the plate thickness, the average Mn concentration of the surface layer softened portion is 2.5% by mass or less, and the recrystallization rate of the surface layer of the surface layer softened portion is It is 90% or more, and the average crystal grain size of the recrystallized structure in the softened part of the surface layer is 0.1 μm or more and 40 μm or less. (2) The high-strength steel sheet according to the above (1), wherein the center portion of the aforementioned plate thickness is contained in mass%: C: more than 0.05% and less than 0.80%, Si: 0.001% and more and less than 3.50%, and Mn: more than 4.0% And less than 10.0%, P: 0.10% or less, S: 0.010% or less, sol.Al: 0.001% or more and less than 3.00%, and N: less than 0.050%, and the remainder is composed of iron and unavoidable impurities. (3) The high-strength steel sheet according to the above (2), wherein the center portion of the aforementioned plate thickness includes at least one element selected from the group consisting of: Cr: 0.01% or more and 2.00% or less, Mo: 0.01% or more and 2.00% or less, Cu: 0.01% or more and 2.00% or less, and Ni: 0.01% or more and 2.00% or less. (4) The high-strength steel sheet according to (2) or (3) above, wherein the center of the thickness of the aforementioned plate further includes at least one element selected from the group consisting of: Ti: 0.005% or more and 0.30% or less, Nb: 0.005% or more and 0.30% or less, V: 0.005% or more and 0.30% or less, and W: 0.005% or more and 0.30% or less. (5) The high-strength steel sheet according to any one of (2) to (4) above, wherein the center portion of the aforementioned plate thickness includes at least one element selected from the group consisting of: B: 0.0001% or more and 0.010% or less, Ca: 0.0001% or more and 0.010% or less, Mg: 0.0001% or more and 0.010% or less, Zr: 0.0001% or more and 0.010% or less, and REM: 0.0001% or more and 0.010% or less. (6) The high-strength steel sheet according to any one of the above (2) to (5), wherein the central part of the aforementioned plate thickness includes at least one element selected from the group consisting of: Sb: 0.0005% or more and 0.050% or less, Sn: 0.0005% or more and 0.050% or less, and Bi: 0.0005% or more and 0.050% or less. (7) The high-strength steel sheet according to any one of (2) to (6), wherein the amount of C in the softened portion of the surface layer is 0.9 times or less the amount of C in the center portion of the plate thickness. (8) The high-strength steel sheet according to any one of (3) to (7) above, wherein the sum of the amount of Cr and Mo in the softened portion of the surface layer is 0.9 of the sum of the amount of Cr and Mo in the center portion of the plate thickness. Times below. (9) The high-strength steel sheet according to any one of (3) to (8) above, wherein the sum of the amount of Cu and the amount of Ni in the softened portion of the surface layer is 0.9 of the sum of the amount of Cu and the amount of Ni in the center portion of the plate thickness. Times below. (10) The high-strength steel sheet according to any one of (4) to (9) above, wherein the sum of the amount of Ti and the amount of Nb in the softened portion of the surface layer is 0.9 of the sum of the amount of Ti and the amount of Nb in the center portion of the plate thickness Times below. (11) The high-strength steel sheet according to any one of (4) to (10) above, wherein the sum of the amount of V and W in the softened portion of the surface layer is 0.9 of the sum of the amount of V and W in the center portion of the plate thickness. Times below. (12) The high-strength steel sheet according to any one of (5) to (11), wherein the amount of B in the softened portion of the surface layer is 0.9 times or less the amount of B in the center portion of the plate thickness. (13) The high-strength steel sheet according to any one of (1) to (12) above, further comprising a hot-dip galvanized layer, an alloyed hot-dip galvanized layer, or an electro-galvanized layer on the surface of the surface layer softened portion. (14) A method for manufacturing a high-strength steel sheet, which is a method for manufacturing a high-strength steel sheet according to any one of (1) to (13) above; the method for manufacturing the high-strength steel sheet is characterized by including the following steps: One or both sides of the base material steel plate at the center of the plate thickness are laminated to form the steel plate for the surface softening portion of the surface softening portion to form a multilayer steel plate; heating the multilayer steel plate to a heating temperature of 1080 ° C to 1300 ° C, and Hot rolling is carried out at a starting rolling temperature of 800 ° C to 1000 ° C; and within 2 seconds after the finish rolling is finished, the multi-layer steel sheet after the hot rolling is cooled to above 500 ° C and 700 ° C The following; after cooling the multilayer steel sheet to a temperature of 500 ° C or more and 700 ° C or less, it is maintained for 3 seconds or more; after the multilayer steel sheet is maintained at a temperature of 500 ° C or more and 700 ° C or less for 3 seconds or more, Then, cold rolling is performed at a reduction ratio of 20% to 70%; and the multilayer steel sheet after the cold rolling is maintained at a temperature of 600 ° C or higher and 750 ° C or lower for 5 seconds or more, followed by cooling. (15) The method for manufacturing a high-strength steel sheet according to the above (14), wherein the multilayer steel sheet is wound at a coiling temperature of 600 ° C. or lower and held at a temperature of 500 ° C. or higher and 700 ° C. or lower for 3 seconds or longer. (16) The method for manufacturing a high-strength steel sheet according to the above (15), in which the multi-layer steel sheet after coiling is held at a temperature of 300 ° C or higher and 550 ° C or lower and tempered before the cold rolling.

發明效果 根據本發明,可提供一種具有優異之強度、延展性平衡,並且具有優異彎曲特性且含Mn濃度高之高強度鋼板。Effects of the Invention According to the present invention, it is possible to provide a high-strength steel sheet having an excellent balance of strength and ductility, excellent bending characteristics, and a high Mn-containing concentration.

發明實施形態 以下針對本發明之實施形態進行說明。此外,本發明不受限於以下實施形態。Embodiments of the Invention Embodiments of the invention will be described below. The present invention is not limited to the following embodiments.

1.表層軟化部之構成 說明以上述方式規定本發明鋼板之構成的理由。以下的說明中,在未特別說明的前提下,表示各元素含量之「%」係指質量%。1. Structure of Surface Softening Section The reason why the structure of the steel sheet of the present invention is specified in the above manner will be explained. In the following description, unless otherwise specified, "%" indicating the content of each element means mass%.

本發明鋼板之表層軟化部的平均Mn濃度必須為2.5質量%以下且再結晶率必須為90%以上,且該表層軟化部具有板厚之0.1%到30%的厚度。The average Mn concentration of the surface layer softened portion of the steel sheet of the present invention must be 2.5% by mass or less and the recrystallization rate must be 90% or more. The surface layer softened portion has a thickness of 0.1% to 30% of the plate thickness.

(表層軟化部之厚度為0.1%以上且30%以下) 表層軟化部之厚度若小於板厚之0.1%則彎曲性無法充分獲得改善,而若大於30%則拉伸強度之劣化會變得明顯。表層軟化部之厚度較佳為板厚的20%以下,更佳為10%以下。(The thickness of the softened portion of the surface layer is 0.1% to 30%) If the thickness of the softened portion of the surface layer is less than 0.1% of the plate thickness, the bendability cannot be sufficiently improved, and if it is more than 30%, the deterioration of tensile strength will become obvious. . The thickness of the surface softened portion is preferably 20% or less of the plate thickness, and more preferably 10% or less.

「表層軟化部」係如以下來決定。首先,以硝太蝕劑腐蝕而使鋼板之截面組織露出,並根據由光學顯微鏡或掃描型電子顯微鏡觀察而得之組織影像,來算出鋼板之總厚度。於鋼板之板厚方向的中心,在相對於板厚方向呈垂直方向上以壓痕互不干涉之衝印間隔針對5點以壓入荷重100g重來測定維氏硬度,並以該等之平均值作為板厚方向之中心位置上的平均維氏硬度。其次,由板厚方向之中心朝向表面,將衝印間隔設為鋼板之總厚度5%的固定間隔,並在各自之板厚方向位置上,與上述同樣地進行5點之維氏硬度試驗。當某板厚方向位置上之平均維氏硬度為板厚方向之中心位置上之平均維氏硬度的0.6倍以下時,將較該位置更靠表面側定義為表層軟化部。當以5%間隔之衝印無法獲得平均維氏硬度的0.6倍以下之值而無法定義表層軟化部時,係藉由在表層之2衝印點之間,以縮得較最初衝印的間隔更短的任意固定間隔進行衝印,以定義表層軟化部。The "surface softening part" is determined as follows. First, the cross-section structure of the steel plate is exposed by the nitrate etchant, and the total thickness of the steel plate is calculated from the structure image obtained by observation with an optical microscope or a scanning electron microscope. The Vickers hardness is measured at the center of the plate thickness direction of the steel plate at a punching interval that does not interfere with each other in a direction perpendicular to the plate thickness direction. The Vickers hardness is measured at a pressure of 100 g for 5 points and the average of these is used. The value is taken as the average Vickers hardness at the center position in the thickness direction. Next, from the center of the plate thickness direction to the surface, the punching interval is set to a fixed interval of 5% of the total thickness of the steel plate, and the Vickers hardness test at 5 points is performed at the same position in the plate thickness direction as described above. When the average Vickers hardness at a position in the thickness direction is 0.6 times or less the average Vickers hardness at the center position in the thickness direction, the surface side softer than the position is defined as the surface layer softened portion. When printing at a 5% interval cannot obtain a value less than 0.6 times the average Vickers hardness and cannot define the surface softened portion, the interval between the two printed points on the surface is used to reduce the interval from the initial printing. Print at any shorter fixed interval to define the surface softening.

(表層軟化部之平均Mn濃度為2.5質量%以下) Mn係可助長帶狀組織之形成的元素。若表層軟化部之平均Mn濃度大於2.5質量%,在表層軟化部就會有帶狀組織形成,而無法獲得良好之彎曲性。因此,表層軟化部之平均Mn濃度係設為2.5質量%以下,且宜設為2.0質量%以下,較佳係設為1.5質量%以下。由於Mn量越少帶狀組織會變得越難形成,因此平均Mn濃度之下限並無特別規定。又,「表層軟化部之平均Mn濃度」是在組織截面之板厚方向中心,沿著與板厚方向呈垂直方法之線上,以50μm間隔利用EPMA測定20點之Mn濃度,並由其平均值求取。(The average Mn concentration in the softened portion of the surface layer is 2.5% by mass or less) Mn is an element that promotes the formation of a band-like structure. If the average Mn concentration in the surface layer softened portion is more than 2.5% by mass, a band-like structure is formed in the surface layer softened portion, and good bendability cannot be obtained. Therefore, the average Mn concentration in the surface softened portion is set to 2.5% by mass or less, preferably 2.0% by mass or less, and more preferably 1.5% by mass or less. Since the band-shaped structure becomes more difficult to form as the amount of Mn decreases, the lower limit of the average Mn concentration is not particularly limited. In addition, the "average Mn concentration in the surface softened portion" is measured at the center of the plate thickness direction of the tissue cross section along a line perpendicular to the plate thickness direction by EPMA at 50 μm intervals at 20 points, and the average value is calculated from the average value. Seeking.

(表層軟化部之再結晶率為90%以上) 若表層之再結晶不充分且有未再結晶組織存在,則因未再結晶組織之延展性貧乏而在彎曲變形時會成為破裂的起點。若表層軟化部之再結晶率小於90%便無法獲得良好彎曲性,因此表層軟化部之再結晶率係設為90%以上。且較佳是在95%以上。(The recrystallization rate of the softened part of the surface layer is 90% or more.) If the recrystallization of the surface layer is insufficient and an unrecrystallized structure is present, it will become a starting point of cracking during bending due to poor ductility of the unrecrystallized structure. If the recrystallization rate of the surface layer softened portion is less than 90%, good bendability cannot be obtained, so the recrystallization rate of the surface layer softened portion is set to 90% or more. And it is preferably at least 95%.

(表層軟化部之平均結晶粒徑為0.1μm以上且40μm以下) 若表層之再結晶組織(肥粒鐵)的平均結晶粒徑粗大化,便會於彎曲變形時助長變形的不均勻化,因而成為彎曲性劣化的主要原因。因此,表層軟化部之平均結晶粒徑係設為40μm以下。且表層軟化部之平均結晶粒徑較佳為30μm以下,更佳為25μm以下。另一方面,若平均結晶粒徑變成0.1μm以下,表層軟化部之延展性會明顯劣化,因此表層軟化部之平均結晶粒徑係設為0.1μm以上。且表層軟化部之平均結晶粒徑較佳為0.5 μm以上,更佳為1μm以上。(The average crystal grain size in the softened part of the surface layer is 0.1 μm or more and 40 μm or less) If the average crystal grain size of the recrystallized structure (ferrous iron) in the surface layer is coarsened, the unevenness of deformation is promoted during bending deformation, so that It becomes a main cause of deterioration of flexibility. Therefore, the average crystal grain size of the surface layer softened portion is set to 40 μm or less. The average crystal grain size of the softened portion of the surface layer is preferably 30 μm or less, and more preferably 25 μm or less. On the other hand, if the average crystal grain size becomes 0.1 μm or less, the ductility of the surface layer softened portion is significantly deteriorated. Therefore, the average crystal grain size of the surface layer softened portion is set to 0.1 μm or more. The average crystal grain size of the softened portion of the surface layer is preferably 0.5 μm or more, and more preferably 1 μm or more.

「再結晶率」係如下進行而決定。在以SEM/EBSD法進行之再結晶率測定試驗中,對鋼板表面施行鏡面研磨及膠體研磨,使根據上述方法定義之表層軟化部之厚度方向的中央位置成為測定面,並使用場發射掃描式電子顯微鏡(FE-SEM)及OIM結晶方位解析裝置,在測定面100μm平方的區域中以0.2μm間隔取得結晶方位資料群。以解析軟體(TSL OIM Analysis)解析所得之結晶方位資料群,並將第一接近測定點間之Kernel Average Misorientation(KAM值)為1.0°以下的區域定義為再結晶組織,並算出該區域之相對於總區域的面積率。The "recrystallization rate" is determined as follows. In the recrystallization rate measurement test by the SEM / EBSD method, the surface of the steel plate is subjected to mirror polishing and colloidal polishing, so that the center position in the thickness direction of the surface softening portion defined by the above method becomes the measurement surface, and a field emission scanning method is used. An electron microscope (FE-SEM) and an OIM crystal orientation analysis device acquire crystal orientation data groups at intervals of 0.2 μm in a 100 μm square area of the measurement surface. An analysis software (TSL OIM Analysis) was used to analyze the crystal orientation data group, and the area where the Kernel Average Misorientation (KAM value) between the first measurement points was 1.0 ° or less was defined as the recrystallized structure, and the relative area of the area was calculated. The area ratio of the total area.

表層軟化部之平均結晶粒徑係如下進行而決定。在以SEM/EBSD法進行之平均結晶粒徑測定試驗中,利用解析軟體(TSL OIM Analysis)解析以上述方法所得之結晶方位資料群,再藉由Area Fraction法算出將具有結晶方位差15°以上之方位差的結晶晶界所包圍的區域定義為一個結晶粒時之粒徑,並算出觀察區域整體之平均粒徑。The average crystal grain size of the surface layer softened portion is determined as follows. In the average crystal particle size measurement test by the SEM / EBSD method, the crystal orientation data group obtained by the above method was analyzed by using an analysis software (TSL OIM Analysis), and the crystal orientation difference was calculated by the Area Fraction method to be 15 ° or more. The area surrounded by the crystal grain boundaries of the azimuth difference is defined as the particle size of one crystal grain, and the average particle size of the entire observation area is calculated.

2.板厚中心部之化學組成 接下來,說明用以獲得本發明效果之較佳板厚中心部(中心層)之化學組成。另,有關元素含量之「%」只要無特別定義即指「質量%」。2. Chemical composition of plate thickness center portion Next, the chemical composition of the plate thickness center portion (center layer) for obtaining the effect of the present invention will be described. In addition, as long as there is no special definition of "%" regarding element content, it means "mass%".

(C:大於0.05%且小於0.80%) 在用以提高鋼的強度並確保殘留沃斯田鐵上,C是極為重要的元素。為了保持充分的強度並獲得殘留沃斯田鐵量,C含量必須大於0.05%以上。另一方面,當含有過量的C時會損及鋼板的熔接性,故將C含量上限設為小於0.80%。C含量宜在0.60%以下之範圍,且以在0.50%以下之範圍為佳。(C: more than 0.05% and less than 0.80%) C is an extremely important element in order to improve the strength of the steel and ensure the residual Vosted iron. In order to maintain sufficient strength and obtain a residual amount of iron in Wastfield, the C content must be greater than 0.05%. On the other hand, when excessive C is contained, the weldability of the steel sheet is impaired, so the upper limit of the C content is set to less than 0.80%. The C content is preferably in a range of 0.60% or less, and more preferably in a range of 0.50% or less.

(Si:0.001%以上且小於3.50%) 對於強化回火麻田散鐵並將組織均勻化以改善加工性,Si係有效元素。並且,Si也具有抑制雪明碳鐵析出並促進沃斯田鐵殘留的作用。為了獲得上述效果,必須有0.001%以上之Si含量。另一方面,當含有過量的Si時會損及鋼板的低溫韌性,故將Si含量之上限值設為小於3.50%。Si之下限值宜為0.01%,較佳為0.30%,更佳為0.50%。藉由令Si含量之下限值在上述範圍中,便可更加提升鋼板的均勻延伸特性。而Si含量之上限值宜為3.00%,較佳為2.50%。(Si: 0.001% or more and less than 3.50%) Si is an effective element for strengthening tempered Asada iron and homogenizing the structure to improve workability. In addition, Si also has the effect of suppressing the precipitation of cis-carbon iron and promoting the retention of Vostian iron. In order to obtain the above effect, it is necessary to have a Si content of 0.001% or more. On the other hand, when excessive Si is contained, the low temperature toughness of the steel sheet is impaired, so the upper limit of the Si content is set to less than 3.50%. The lower limit of Si is preferably 0.01%, preferably 0.30%, and more preferably 0.50%. By setting the lower limit of the Si content within the above range, the uniform elongation characteristics of the steel sheet can be further improved. The upper limit of the Si content is preferably 3.00%, and more preferably 2.50%.

(Mn:大於4.00%且小於10.0%) Mn係可使沃斯田鐵穩定化並提高淬火性之元素。此外,本發明之鋼板中,係使Mn分配在沃斯田鐵中,以使沃斯田鐵更加穩定化。為了要在室溫下使沃斯田鐵穩定化,必須有大於4.00%的Mn。另一方面,若鋼板含有過量之Mn便會損及低溫韌性,因此將Mn含量上限設為小於10.0%。Mn含量之下限值宜為4.30%,較佳為4.80%。且Mn含量之上限值宜為8.00%,較佳為7.50%。藉由令Mn含量之下限值及上限值在上述範圍內,便可更加穩定地獲得延展性。又,「板厚中心部之平均Mn濃度」是在組織截面之板厚中心部的板厚方向中心,沿著與板厚方向呈垂直方法之線上,以50μm間隔利用EPMA測定20點之Mn濃度,並由其平均值求取。(Mn: more than 4.00% and less than 10.0%) Mn is an element that stabilizes Vosstian iron and improves hardenability. In addition, in the steel sheet of the present invention, Mn is distributed in the Vosstian iron to stabilize the Vosstian iron. In order to stabilize Vosstian iron at room temperature, it is necessary to have Mn greater than 4.00%. On the other hand, if the steel sheet contains excessive Mn, the low-temperature toughness is impaired. Therefore, the upper limit of the Mn content is set to less than 10.0%. The lower limit of the Mn content is preferably 4.30%, and more preferably 4.80%. The upper limit of the Mn content is preferably 8.00%, and more preferably 7.50%. By setting the lower limit value and the upper limit value of the Mn content within the above range, the ductility can be obtained more stably. The "average Mn concentration at the center of the plate thickness" refers to the center of the plate thickness direction at the center of the plate thickness of the tissue cross section, along the line perpendicular to the plate thickness direction, and measured the Mn concentration at 20 points by EPMA at 50 μm intervals. And calculate from its average.

(sol.Al:0.001%以上且小於3.00%) Al為去氧劑,必須含有0.001%以上。並且,由於Al會擴展退火時之二相溫度區,因此也有提高材質穩定性的作用。雖然Al含量越多該效果會變得越大,但若含有過量的Al,便會招致表面性狀、塗裝性及熔接性等劣化,故將sol.Al的上限設為小於3.00%。sol.Al含量之下限值宜為0.005%,較佳為0.01%,更佳為0.02%。且sol.Al含量之上限值宜為2.50%,較佳為1.80%。藉由令sol.Al含量之下限值及上限值在上述範圍內,去氧效果及提升材質穩定之效果與表面性狀、塗裝性以及熔接性之平衡會變得更加良好。(sol.Al: 0.001% or more and less than 3.00%) Al is a deoxidizer and must contain 0.001% or more. In addition, since Al expands the two-phase temperature range during annealing, it also has the effect of improving material stability. Although the effect becomes larger as the content of Al increases, if excessive Al is contained, surface properties, paintability, and weldability are deteriorated. Therefore, the upper limit of sol.Al is set to less than 3.00%. The lower limit of the sol.Al content is preferably 0.005%, preferably 0.01%, and more preferably 0.02%. And the upper limit of the sol.Al content should be 2.50%, more preferably 1.80%. By setting the lower limit value and the upper limit value of the sol.Al content within the above range, the balance between the deoxidizing effect and the effect of improving the stability of the material and the surface properties, paintability and weldability will become better.

(P:0.10%以下) P為不純物,若鋼板含有過量之P便會損害韌性及熔接性。因此,令P含量上限為0.10%以下。P含量之上限值宜為0.050%,較佳為0.030%,更佳為0.020%。因本實施形態之鋼板不一定要有P,故P含量之下限值為0.000%。P含量之下限值可為大於0.000%或亦可為0.001%,但P含量越少越好。(P: 0.10% or less) P is an impurity. If the steel sheet contains excessive P, the toughness and weldability will be impaired. Therefore, the upper limit of the P content is set to 0.10% or less. The upper limit of the P content is preferably 0.050%, preferably 0.030%, and more preferably 0.020%. Since the steel sheet of this embodiment does not necessarily have P, the lower limit of the P content is 0.000%. The lower limit of the P content may be greater than 0.000% or 0.001%, but the smaller the P content, the better.

(S:0.010%以下) S為不純物,若鋼板含有過量之S便會因熱軋延而生成伸長的MnS,而招致彎曲性及擴孔性等成形性劣化。因此,將S含量上限設為0.010%以下。S含量之上限值宜為0.007%,較佳為0.003%。因本實施形態之鋼板不一定要有S,故S含量之下限值為0.000%。S含量之下限值可設為大於0.000%或亦可設為0.0001%,但S含量越少越好。(S: 0.010% or less) S is an impure substance. If the steel sheet contains excessive S, hot-rolling will generate elongated MnS, resulting in deterioration of bendability and formability such as hole expandability. Therefore, the upper limit of the S content is set to 0.010% or less. The upper limit of the S content is preferably 0.007%, and more preferably 0.003%. Since the steel sheet of this embodiment does not necessarily need to have S, the lower limit of the S content is 0.000%. The lower limit of the S content can be set to greater than 0.000% or 0.0001%, but the smaller the S content, the better.

(N:小於0.050%) N為不純物,若鋼板含有0.050%以上之N便會招致韌性劣化。因此,將N含量上限設為小於0.050%。且N含量之上限值宜為0.010%,較佳為0.006%。因本實施形態之鋼板不一定要有N,故N含量之下限值為0.000%。N含量之下限值可設為大於0.000%或亦可設為0.0003%,但N含量越少越好。(N: less than 0.050%) N is an impurity, and if the steel sheet contains N in an amount of 0.050% or more, the toughness will be deteriorated. Therefore, the upper limit of the N content is set to less than 0.050%. The upper limit of the N content is preferably 0.010%, and more preferably 0.006%. Since the steel sheet of this embodiment does not necessarily have N, the lower limit of the N content is 0.000%. The lower limit of the N content may be set to be greater than 0.000% or may be set to 0.0003%, but the smaller the N content, the better.

(Cr:0.01%以上且2.00%以下、Mo:0.01%以上且2.00%以下、Cu:0.01%以上且2.00%以下及Ni:0.01%以上且2.00%以下) 對本實施形態之鋼板而言,Cr、Mo、Cu及Ni分別皆非必要元素。但是,由於Cr、Mo、Cu及Ni係可提升鋼板強度的元素,故亦可含有。為了獲得提升鋼板強度之效果,鋼板亦可分別含有0.01%以上選自於由Cr、Mo、Cu及Ni所構成群組中的1種或2種以上元素。然而,若鋼板含有過量之該等元素,便容易生成熱軋時之表面傷痕,而且會有熱軋鋼板之強度變得過高而冷軋延性降低的情況。因此,將選自於由Cr、Mo、Cu及Ni所構成群組中的1種或2種以上元素各自的含量上限值設為2.00%。(Cr: 0.01% or more and 2.00% or less, Mo: 0.01% or more and 2.00% or less, Cu: 0.01% or more and 2.00% or less and Ni: 0.01% or more and 2.00% or less) For the steel sheet of this embodiment, Cr , Mo, Cu, and Ni are not essential elements, respectively. However, since Cr, Mo, Cu, and Ni are elements which can increase the strength of the steel sheet, they may also be contained. In order to obtain the effect of improving the strength of the steel sheet, the steel sheet may also contain at least 0.01% of one or more elements selected from the group consisting of Cr, Mo, Cu, and Ni. However, if the steel sheet contains excessive amounts of these elements, it is easy to generate surface flaws during hot rolling, and the strength of the hot rolled steel sheet may become too high and the cold rolling ductility may be reduced. Therefore, the upper limit of the content of each of one or more elements selected from the group consisting of Cr, Mo, Cu, and Ni is set to 2.00%.

(Ti:0.005%以上且0.30%以下、Nb:0.005%以上且0.30%以下、V:0.005%以上且0.30%以下及W:0.005%以上且0.30%以下) 對本實施形態之鋼板而言,Ti、Nb、V及W並非必要元素。然而,Ti、Nb、V及W係可生成微細碳化物、氮化物或碳氮化物之元素,故對提升鋼板強度係為有效。因此,鋼板亦可含有選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素。為了獲得提升鋼板強度之效果,宜將選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素之各自含量之下限值設為0.005%。另一方面,若含有過量的該等元素,便會有熱軋鋼板強度過度上升而冷軋延性降低的情況。因此,將選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素各自的含量上限值設為0.30%。(Ti: 0.005% or more and 0.30% or less, Nb: 0.005% or more and 0.30% or less, V: 0.005% or more and 0.30% or less and W: 0.005% or more and 0.30% or less) For the steel sheet of this embodiment, Ti , Nb, V, and W are not essential elements. However, Ti, Nb, V, and W are elements that can form fine carbides, nitrides, or carbonitrides, and are therefore effective for improving the strength of steel sheets. Therefore, the steel sheet may contain one or more elements selected from the group consisting of Ti, Nb, V, and W. In order to obtain the effect of improving the strength of the steel sheet, the lower limit of the respective content of one or more elements selected from the group consisting of Ti, Nb, V, and W should be set to 0.005%. On the other hand, if these elements are contained excessively, the strength of the hot-rolled steel sheet may increase excessively and the cold-rolled ductility may decrease. Therefore, the upper limit of the content of each of one or more elements selected from the group consisting of Ti, Nb, V, and W is set to 0.30%.

(B:0.0001%以上且0.010%以下、Ca:0.0001%以上且0.010%以下、Mg:0.0001%以上且0.010%以下、Zr:0.0001%以上且0.010%以下及REM:0.0001%以上且0.010%以下) B、Ca、Mg、Zr及REM並非必要元素。然而,B、Ca、Mg、Zr及REM會使鋼板之局部延展性及擴孔性提升。為了獲得該效果,宜將選自於由B、Ca、Mg、Zr及REM所構成群組中的1種或2種以上元素各自的下限值設為0.0001%,較佳是設為0.001%。但是,過量之該等元素會使鋼板之加工性劣化,因此該等元素各自之含量上限宜設為0.010%以下,且選自於由B、Ca、Mg、Zr及REM所構成群組中的1種或2種以上元素的含量合計宜設為0.030%以下。(B: 0.0001% or more and 0.010% or less, Ca: 0.0001% or more and 0.010% or less, Mg: 0.0001% or more and 0.010% or less, Zr: 0.0001% or more and 0.010% or less and REM: 0.0001% or more and 0.010% or less ) B, Ca, Mg, Zr and REM are not essential elements. However, B, Ca, Mg, Zr and REM will improve the local ductility and hole expandability of the steel sheet. In order to obtain this effect, the lower limit of one or two or more elements selected from the group consisting of B, Ca, Mg, Zr, and REM should preferably be 0.0001%, preferably 0.001%. . However, an excessive amount of these elements will deteriorate the workability of the steel sheet. Therefore, the upper limit of the content of each of these elements should be set to 0.010% or less, and it is selected from the group consisting of B, Ca, Mg, Zr, and REM. The total content of one or more elements should preferably be 0.030% or less.

(Sb:0.0005%以上且0.050%以下、Sn:0.0005%以上且0.050%以下及Bi:0.0005%以上且0.050%以下) Sb、Sn及Bi並非必要元素。然而,Sb、Sn及Bi會抑制鋼板中的Mn、Si及/或Al等易氧化元素擴散至鋼板表面形成氧化物,而可提高鋼板的表面性狀及鍍敷性。為了獲得該效果,宜將選自於由Sb、Sn及Bi所構成群組中的1種或2種以上元素各自的含量下限值設為0.0005%,較佳是設為0.001%。另一方面,若該等元素各自的含量大於0.050%,該效果便會飽和,故將該等元素各自的含量上限值設為0.050%。(Sb: 0.0005% or more and 0.050% or less, Sn: 0.0005% or more and 0.050% or less and Bi: 0.0005% or more and 0.050% or less) Sb, Sn, and Bi are not essential elements. However, Sb, Sn, and Bi inhibit the diffusion of oxidizable elements such as Mn, Si, and / or Al to the surface of the steel sheet to form oxides, and can improve the surface properties and plating properties of the steel sheet. In order to obtain this effect, the lower limit of the content of each of the one or two or more elements selected from the group consisting of Sb, Sn, and Bi is preferably set to 0.0005%, and preferably 0.001%. On the other hand, if the content of each of these elements is greater than 0.050%, the effect is saturated, so the upper limit of the content of each of these elements is set to 0.050%.

3.表層軟化部之化學組成 就Mn以外之元素而言,本發明之鋼板也會有在表層軟化部與板厚中心部中化學組成不同的情況。為所述情況時,表層軟化部之較佳化學組成如下。3. Chemical composition of the surface softened portion As far as elements other than Mn are concerned, the steel sheet of the present invention may have different chemical compositions in the surface softened portion and the thickness center portion. In this case, the preferable chemical composition of the surface softened portion is as follows.

(C:板厚中心部之C量的0.9倍以下) C係可提高鋼板強度之元素,係用以提高高強度鋼板之強度而添加。表層軟化部之C量宜為板厚中心部之C量的0.9倍以下。其係因要將表層軟化部之硬度降得比板厚中心部之硬度還低之故。若大於0.9倍,便會有無法獲得優異彎曲性的情況。較佳為表層軟化部之C量為板厚中心部之C量的0.7倍以下,在0.5倍以下更佳,又以0.3倍以下最佳。由於板厚中心部之較佳C含量為小於0.80%,故表層軟化部之較佳C含量為小於0.72%。且宜為小於0.5%,小於0.3%更佳,又以小於0.1%最佳。C量的下限並無特別規定。當使用工業用之極低C鋼時,其實質下限為0.001%左右,但由所謂固溶C量之觀點來看,亦可利用使用Ti或Nb等而完全排除固溶C之Interstitial Free鋼。(C: 0.9 times or less the amount of C in the center of the plate thickness) C is an element that can increase the strength of the steel sheet and is added to increase the strength of the high-strength steel sheet. The amount of C in the softened portion of the surface layer should be 0.9 times or less the amount of C in the center portion of the plate thickness. The reason is to reduce the hardness of the softened portion of the surface layer to be lower than that of the center portion of the plate thickness. If it is more than 0.9 times, excellent bendability may not be obtained. The amount of C in the softened portion of the surface layer is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less. Since the preferred C content in the central portion of the plate thickness is less than 0.80%, the preferred C content in the surface softened portion is less than 0.72%. It should be less than 0.5%, more preferably less than 0.3%, and most preferably less than 0.1%. The lower limit of the amount of C is not particularly specified. When extremely low C steel for industrial use is used, the actual lower limit is about 0.001%. However, from the viewpoint of the so-called solid solution C amount, Interstitial Free steel that completely excludes solid solution C can also be used by using Ti or Nb.

(Si:0.001%以上且小於3.50%) Si係肥粒鐵穩定化元素,因可增加Ac3變態點故可在廣泛的退火溫度下形成大量的肥粒鐵,而以改善組織控制性之觀點作添加。為獲得所述效果,必須設Si量在0.001%以上。然而,添加3.50%以上會使鋼板之表面性狀劣化,因此設其為小於3.50%。(Si: 0.001% or more and less than 3.50%) The Si-based ferrous iron stabilizing element can increase the Ac3 abnormality point, so that a large amount of ferrous iron can be formed at a wide range of annealing temperatures. Add to. In order to obtain the effect, the amount of Si must be set to 0.001% or more. However, the addition of 3.50% or more deteriorates the surface properties of the steel sheet, so it is set to less than 3.50%.

(P:0.10%以下) P會使熔接部脆化。若大於0.10%則熔接部脆化會變顯著,故將其適當範圍限定在0.10%以下。雖未規定P含量的下限,但若設為小於0.001%則於經濟層面來說不利。(P: 0.10% or less) P embrittles the welded portion. If it is more than 0.10%, the embrittlement of the welded portion becomes significant, so the appropriate range is limited to 0.10% or less. Although the lower limit of the P content is not specified, if it is set to less than 0.001%, it is economically disadvantageous.

(S:0.010%以下) S會對熔接性以及鑄造時及熱軋時之製造性帶來不好的影響。由此看來,設其上限値為0.010%以下。雖未規定S含量的下限,但若設為小於0.0001%則於經濟層面來說不利。(S: 0.010% or less) S adversely affects weldability and manufacturability during casting and hot rolling. From this, the upper limit 设 is set to 0.010% or less. Although the lower limit of the S content is not specified, if it is set to less than 0.0001%, it is economically disadvantageous.

(sol.Al:0.001%以上且小於3.00%) Al可作為脫氧劑發揮作用,而宜於脫氧步驟添加。為獲得所述效果,必須使sol.Al含量在0.001%以上。另一方面,當sol.Al含量為3.00%以上時,連續鑄造時之鋼胚破裂的危險性會升高,因此設其為小於3.00%。(sol.Al: 0.001% or more and less than 3.00%) Al can function as a deoxidizing agent, and it is suitable to be added in the deoxidizing step. In order to obtain the effect, the sol.Al content must be 0.001% or more. On the other hand, when the sol.Al content is 3.00% or more, the risk of cracking of the steel billet during continuous casting increases, so it is set to less than 3.00%.

(N:0.050%以下) N會形成粗大氮化物致使彎曲性變差,故須抑制添加量。其係因若N大於0.050%則該傾向會變顯著,故設N含量範圍在0.050%以下。並且,N會致使於熔接時產生氣孔故宜少。N含量的下限値並無特別限定而可發揮本發明之效果,但若設N含量為小於0.0005%,則會導致製造成本大幅增加。(N: 0.050% or less) N forms coarse nitrides and deteriorates bendability. Therefore, the amount of N must be suppressed. The reason is that if N is greater than 0.050%, the tendency will be significant, so the N content range is set to 0.050% or less. In addition, N should cause fewer pores during welding. The lower limit 値 of the N content is not particularly limited so that the effects of the present invention can be exerted, but if the N content is set to less than 0.0005%, the manufacturing cost will increase significantly.

表層軟化部宜具有如下組成: 以質量%計含有: C:小於0.72%、 Si:0.001%以上且小於3.50%、 Mn:2.5%以下、 P:0.10%以下、 S:0.010%以下、 sol.Al:0.001%以上且小於3.00%、及 N:小於0.050%,且 剩餘部分由鐵及無法避免之不純物所構成。表層軟化部可更含有下述成分。The surface softening section preferably has the following composition: Contained in mass%: C: less than 0.72%, Si: 0.001% or more and less than 3.50%, Mn: 2.5% or less, P: 0.10% or less, S: 0.010% or less, sol. Al: 0.001% or more and less than 3.00%, and N: less than 0.050%, and the remainder is composed of iron and unavoidable impurities. The surface layer softened portion may further contain the following components.

(Cr:0.01%以上且2.00%以下、Mo:0.01%以上且2.00%以下、Cu:0.01%以上且2.00%以下及Ni:0.01%以上且2.00%以下) Cr、Mo、Cu及Ni係可提升鋼板強度的元素,故亦可含有。鋼板亦可分別含有0.01%以上之選自於由Cr、Mo、Cu及Ni所構成群組中的1種或2種以上元素。然而,若使鋼板含有過量之該等元素,會有鋼板之強度變得過高而變得容易在軋延時生成表面傷痕的情況。因此,將選自於由Cr、Mo、Cu及Ni所構成群組中的1種或2種以上元素各自的含量上限值設為2.00%。(Cr: 0.01% or more and 2.00% or less, Mo: 0.01% or more and 2.00% or less, Cu: 0.01% or more and 2.00% or less and Ni: 0.01% or more and 2.00% or less) Cr, Mo, Cu, and Ni are acceptable It can also contain elements that increase the strength of the steel sheet. The steel sheet may contain 0.01% or more of one or more elements selected from the group consisting of Cr, Mo, Cu, and Ni, respectively. However, if the steel sheet contains excessive amounts of these elements, the strength of the steel sheet may become too high, and it may become easy to generate surface flaws during rolling delay. Therefore, the upper limit of the content of each of one or more elements selected from the group consisting of Cr, Mo, Cu, and Ni is set to 2.00%.

又,表層軟化部之Cr量及Mo量的總和宜設為板厚中心部之Cr量及Mo量的總和的0.9倍以下。會使碳化物穩定化之Cr量與Mo量的總和若大於板厚中心部之Cr量及Mo量的0.9倍,則粗大碳化物容易殘存,而會成為表面性狀劣化的原因。其較佳為0.7倍以下,更佳為0.5倍以下,又以0.3倍以下最佳。The total amount of Cr and Mo in the surface softened portion is preferably 0.9 times or less of the total amount of Cr and Mo in the center portion of the plate thickness. If the sum of the amount of Cr and Mo that stabilizes carbides is greater than 0.9 times the amount of Cr and Mo in the center of the plate thickness, coarse carbides tend to remain and cause surface deterioration. It is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less.

又,表層軟化部之Cu量及Ni量的總和宜設為板厚中心部之Cu量及Ni量的總和的0.9倍以下。可改善淬火性之Cu量及Ni量的總和若大於板厚中心部之Cu量及Ni量的0.9倍,則易產生低溫變態組織,而會成為彎曲性劣化的原因。其較佳為0.7倍以下,更佳為0.5倍以下,又以0.3倍以下最佳。The sum of the amount of Cu and the amount of Ni in the surface softened portion should preferably be 0.9 times or less the sum of the amount of Cu and the amount of Ni in the center portion of the plate thickness. If the sum of the amount of Cu and Ni that can improve the hardenability is greater than 0.9 times the amount of Cu and Ni in the center of the plate thickness, a low-temperature deformed structure is likely to occur, which may cause the deterioration of bendability. It is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less.

(Ti:0.005%以上且0.30%以下、Nb:0.005%以上且0.30%以下、V:0.005%以上且0.30%以下及W:0.005%以上且0.30%以下) Ti、Nb、V及W係可生成微細碳化物、氮化物或碳氮化物之元素,故對提升鋼板強度係為有效。因此,鋼板亦可含有選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素。為了獲得提升鋼板強度之效果,宜將選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素各自的含量下限值設為0.005%。另一方面,若含有過量的該等元素,熱軋鋼板之強度會過度上升而有在冷軋延時破裂的可能性。因此,將選自於由Ti、Nb、V及W所構成群組中的1種或2種以上元素各自的含量上限值設為0.30%。(Ti: 0.005% or more and 0.30% or less, Nb: 0.005% or more and 0.30% or less, V: 0.005% or more and 0.30% or less and W: 0.005% or more and 0.30% or less) Ti, Nb, V, and W are acceptable An element that generates fine carbides, nitrides, or carbonitrides is effective for improving the strength of steel sheets. Therefore, the steel sheet may contain one or more elements selected from the group consisting of Ti, Nb, V, and W. In order to obtain the effect of improving the strength of the steel sheet, the lower limit value of each content of one or two or more elements selected from the group consisting of Ti, Nb, V, and W should be 0.005%. On the other hand, if these elements are contained excessively, the strength of the hot-rolled steel sheet may be excessively increased, and there is a possibility of cracking during the cold rolling delay. Therefore, the upper limit of the content of each of one or more elements selected from the group consisting of Ti, Nb, V, and W is set to 0.30%.

又,表層軟化部之Ti量及Nb量的總和宜設為板厚中心部之Ti量及Nb量的總和的0.9倍以下。Ti量與Nb量的總和若大於板厚中心部之Ti量及Nb量的0.9倍,則表層容易硬質化,而會成為彎曲性劣化的原因。其較佳為0.7倍以下,更佳為0.5倍以下,又以0.3倍以下最佳。The total amount of Ti and Nb in the surface softened portion should preferably be 0.9 times or less the total amount of Ti and Nb in the center portion of the plate thickness. If the sum of the amount of Ti and the amount of Nb is greater than 0.9 times the amount of Ti and the amount of Nb in the central portion of the plate thickness, the surface layer is likely to be hardened, which may cause the deterioration of bendability. It is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less.

又,表層軟化部之W量及V量的總和宜設為板厚中心部之W量及V量的總和的0.9倍以下。由於W與V為容易形成碳化物之元素,故W量與V量的總和若大於板厚中心部之W量及V量的0.9倍,則表層會有粗大碳化物形成,而會成為彎曲性劣化的主要原因。其較佳為0.7倍以下,更佳為0.5倍以下,又以0.3倍以下最佳。The total amount of W and V in the surface softened portion should preferably be 0.9 times or less the total of the amount of W and V in the center portion of the plate thickness. Since W and V are elements that are liable to form carbides, if the sum of the amount of W and V is greater than 0.9 times the amount of W and V in the center of the plate thickness, coarse carbides will be formed on the surface layer, which will cause bendability. The main cause of deterioration. It is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less.

(B:0.0001%以上且0.010%以下、Ca:0.0001%以上且0.010%以下、Mg:0.0001%以上且0.010%以下、Zr:0.0001%以上且0.010%以下及REM:0.0001%以上且0.010%以下) B、Ca、Mg、Zr及REM會提升鋼板之局部延展性及擴孔性。為了獲得該效果,宜將選自於由B、Ca、Mg、Zr及REM所構成群組中的1種或2種以上元素各自的下限值設為0.0001%,較佳是設為0.001%。另一方面,B、Ca、Mg、Zr及REM量若大於板厚中心部之0.9倍,則表層會過度硬質化,而有使表面性狀劣化的情況。因此,將選自於由B、Ca、Mg、Zr及REM所構成群組中的1種或2種以上元素之上限值設為0.009%,且以設為0.006%以下較佳。(B: 0.0001% or more and 0.010% or less, Ca: 0.0001% or more and 0.010% or less, Mg: 0.0001% or more and 0.010% or less, Zr: 0.0001% or more and 0.010% or less and REM: 0.0001% or more and 0.010% or less ) B, Ca, Mg, Zr and REM will improve the local ductility and hole expansion of the steel plate. In order to obtain this effect, the lower limit of one or two or more elements selected from the group consisting of B, Ca, Mg, Zr, and REM should preferably be 0.0001%, preferably 0.001%. . On the other hand, if the amounts of B, Ca, Mg, Zr, and REM are greater than 0.9 times the center of the plate thickness, the surface layer may be excessively hardened and the surface properties may be deteriorated. Therefore, the upper limit of one or two or more elements selected from the group consisting of B, Ca, Mg, Zr, and REM is set to 0.009%, and more preferably 0.006% or less.

又,表層軟化部之B量宜設為前述板厚中心部之B量的0.9倍以下。B為容易形成低溫變態相的元素,因此若大於板厚中心部之B量的0.9倍則表層會變為硬質,而會成為無法獲得優異彎曲性的原因。其較佳為0.7倍以下,更佳為0.5倍以下,又以0.3倍以下最佳。而該等下限値並無規定。The amount of B in the surface softened portion is preferably 0.9 times or less the amount of B in the center portion of the plate thickness. B is an element that is liable to form a low-temperature metamorphic phase. Therefore, if the amount of B is greater than 0.9 times the amount of B in the center portion of the plate thickness, the surface layer becomes hard, which may cause failure to obtain excellent bendability. It is preferably 0.7 times or less, more preferably 0.5 times or less, and most preferably 0.3 times or less. These lower limits are not required.

4.鋼板之組織 說明本實施形態之鋼板之組織。4. Structure of steel plate The structure of the steel plate in this embodiment will be described.

板厚中心部之組織宜具有由肥粒鐵、麻田散鐵或變韌鐵、以及殘留沃斯田鐵所構成的組織,且較佳係具有由肥粒鐵、回火麻田散鐵或變韌鐵、保持淬火狀態的麻田散鐵、以及殘留沃斯田鐵所構成的組織。The tissue at the center of the plate thickness should have a structure composed of ferrous grain iron, Asada loose iron or toughened iron, and residual Vostian iron, and preferably has a structure consisting of fat iron, tempered Asada iron loosened or toughened Iron, hardened Asada loose iron, and residual Vosted iron.

表層軟化部之組織宜具有實質上由肥粒鐵所構成之組織。The structure of the surface softening portion should preferably have a structure consisting essentially of ferrous iron.

表層軟化部之氣孔率少,且以面積率計宜為1%以下,且實質上為0%更佳。The porosity of the softened portion of the surface layer is small, and is preferably 1% or less in terms of area ratio, and more preferably 0%.

5.鋼板之機械特性 說明本實施形態之鋼板之機械特性。5. Mechanical characteristics of the steel sheet This section describes the mechanical characteristics of the steel sheet of this embodiment.

本實施形態之鋼板的拉伸強度宜在780MPa以上,較佳在1180MPa以上。這是為了在將鋼板作為汽車的胚料使用時,利用高強度化來減少板厚以有助於輕量化。又,為了將本實施形態之鋼板供給至壓製成形,以均勻延伸率(uEL)優異為宜。TS×uEL宜在12000MPa・%以上,較佳是在14000MPa・%以上。The tensile strength of the steel sheet in this embodiment is preferably 780 MPa or more, and more preferably 1180 MPa or more. This is because when a steel sheet is used as a raw material for automobiles, the thickness is reduced by increasing strength to contribute to weight reduction. In addition, in order to supply the steel sheet of this embodiment to press forming, it is preferable to have excellent uniform elongation (uEL). TS × uEL is preferably 12000 MPa ·% or more, and more preferably 14000 MPa ·% or more.

又,關於彎曲性,針對強度為780MPa以上且小於1180MPa的鋼種,以相對於軋延方向呈垂直的方向為長邊方向(彎曲稜線與軋延方向一致)的方式依據JIS Z2248進行V彎曲試驗時,臨界彎曲半徑R宜為1.0mm以下,且較佳為0.8mm以下。針對強度為1180MPa以上之鋼種,上述V彎曲試驗之臨界彎曲半徑宜為2.0mm以下,且較佳為1.5mm以下。Regarding bendability, when performing a V-bend test in accordance with JIS Z2248 for a steel type having a strength of 780 MPa or more and less than 1180 MPa, the direction perpendicular to the rolling direction is taken as the long side direction (the bending ridge line is consistent with the rolling direction). The critical bending radius R is preferably 1.0 mm or less, and preferably 0.8 mm or less. For steel types with a strength of 1180 MPa or more, the critical bending radius of the above-mentioned V-bending test should be 2.0 mm or less, and preferably 1.5 mm or less.

6. 製造方法 接下來說明本實施形態之鋼板之製造方法。以下說明意僅例示用以製得本發明之高強度鋼板之製法,而非意以如下說明之積層有2片鋼板而成之多層鋼板限定本發明之高強度鋼板。例如,亦可取代下述所記載之積層法,而藉由冷噴塗法在母材鋼板上形成表層軟化部。6. Manufacturing method Next, a manufacturing method of the steel plate according to this embodiment will be described. The following description is intended only to illustrate the method for producing the high-strength steel sheet of the present invention, and is not intended to limit the high-strength steel sheet of the present invention to a multi-layer steel sheet formed by laminating two steel sheets as described below. For example, instead of the lamination method described below, a surface layer softened portion may be formed on a base material steel plate by a cold spray method.

本實施形態之鋼板係將多層鋼板熱軋延,並在軋延後即時冷卻且在高溫下保持,然後將已冷卻之鋼板酸洗後,施行冷軋延與退火而製造,前述多層鋼板係在具有上述化學組成且構成板厚中心部的母材鋼板之單面或雙面上,積層平均Mn濃度2.5質量%以下且為上述表層軟化部用鋼板而形成多層鋼板,並熔接其周圍而成。The steel sheet of this embodiment is produced by hot-rolling a multi-layer steel sheet, cooling it immediately after rolling and keeping it at a high temperature, and then pickling the cooled steel sheet, followed by cold-rolling and annealing, to produce the multi-layer steel sheet. The base material steel plate having the above-mentioned chemical composition and constituting the center portion of the plate thickness is formed by laminating an average Mn concentration of 2.5% by mass or less and forming a multilayer steel plate for the steel sheet for the surface layer softening portion, and welding the surroundings.

(多層鋼板的形成:在將構成板厚中心部之表面脫脂後的母材鋼板之單面或雙面上,積層滿足表層軟化部之化學組成的鋼板,並熔接其周圍) 於滿足上述板厚中心部之化學組成的母材鋼板上,將滿足表層軟化部之化學組成的鋼板積層於表面並熔接周圍,藉此以形成多層鋼板。該等鋼板只要滿足上述化學組成,則無論以何種製法製造而得者皆可。(Formation of multi-layer steel plate: On one or both sides of the base material steel plate after degreasing the surface constituting the center portion of the plate thickness, a steel plate satisfying the chemical composition of the surface softening portion is laminated and welded around it.) On the base material steel sheet with the chemical composition in the center part, a steel sheet that satisfies the chemical composition in the surface softening part is laminated on the surface and welded around to form a multilayer steel sheet. As long as these steel plates satisfy the above-mentioned chemical composition, they may be obtained by any manufacturing method.

(多層鋼板之加熱溫度:1080℃以上且1300℃以下) 若熱軋延前之加熱溫度小於1080℃,熱加工時之變形阻力會變高,導致操作變得困難。另一方面,若加熱溫度大於1300℃,便會因氧化皮耗損而導致產率降低。因此,加熱溫度是設為1080℃以上且1300℃以下。在熱軋延前保持於1080℃以上且1300℃以下之溫度區的時間並無特別限定,但為了提升擴孔性,宜設為30分鐘以上,設為1小時以上更佳。且為了抑制過度之氧化皮耗損,宜設為10小時以下,設為5小時以下更佳。又,在進行直送軋延或直接軋延的情況下,保持於上述溫度範圍內並供予熱軋延亦可。本說明書中,溫度係在鋼板表面之中央位置所測定之溫度。(Heating temperature of multilayer steel plate: 1080 ° C or more and 1300 ° C or less) If the heating temperature before hot rolling is less than 1080 ° C, the deformation resistance during hot working becomes high, which makes the operation difficult. On the other hand, if the heating temperature is higher than 1300 ° C, the yield will decrease due to scale wear. Therefore, the heating temperature is set to be 1080 ° C or more and 1300 ° C or less. The time during which the temperature is maintained in the temperature range from 1080 ° C to 1300 ° C before hot rolling is not particularly limited, but in order to improve the hole expandability, it is preferably set to 30 minutes or more, and more preferably 1 hour or more. In addition, in order to suppress excessive scale wear, it should be set to 10 hours or less, and more preferably 5 hours or less. When direct rolling or direct rolling is performed, the rolling may be performed while maintaining the temperature range as described above. In this specification, the temperature is the temperature measured at the center of the surface of the steel sheet.

(精整軋延開始溫度:800℃以上且1000℃以下) 精整軋延開始溫度宜設為800℃以上且在1000℃以下。藉由將精整軋延開始溫度設為800℃以上,便可令軋延時之變形阻力小。另一方面,藉由將精整軋延開始溫度設為1000℃以下,而可抑制因晶界氧化所造成的鋼板表面性狀劣化。(Finishing rolling start temperature: 800 ° C or higher and 1000 ° C or lower) The finishing rolling start temperature is preferably set to 800 ° C or higher and 1000 ° C or lower. By setting the finishing rolling start temperature to 800 ° C or higher, the deformation resistance of the rolling delay can be made small. On the other hand, by setting the finishing rolling start temperature to 1000 ° C. or lower, deterioration of the surface properties of the steel sheet due to grain boundary oxidation can be suppressed.

(軋延後之冷卻:在2秒以內冷卻至500℃以上且700℃以下) 在精整軋延結束後2秒以內,冷卻至500℃以上且700℃以下。此為本發明中很重要的條件,藉由使表層軟化部之舊γ粒微細,並使會於冷卻時生成之肥粒鐵粒均勻微細地生成,而可在後續之退火步驟中,使表層軟化部充分地再結晶。(Cooling after rolling: cooled to 500 ° C or higher and 700 ° C or lower within 2 seconds) Within 2 seconds after finishing rolling, cooled to 500 ° C or higher and 700 ° C or lower. This is a very important condition in the present invention. By making the old γ grains in the softened part of the surface layer fine and uniformly and finely forming the iron particles of the fertilizer particles that will be generated during cooling, the surface layer can be made in the subsequent annealing step. The softened portion was sufficiently recrystallized.

若從精整軋延結束後起算到冷卻至500℃以上且700℃以下的時間大於2秒,舊沃斯田鐵粒徑會變得粗大,在後續之退火步驟中,表層軟化部就不會充分地再結晶。因此,從精整軋延結束後起算到冷卻至500℃以上且700℃以下的時間係設為2秒以內。且宜為1.8秒以內,較佳為1.5秒以內。到冷卻為止的時間越短,舊γ粒徑就會越細粒化而變得容易再結晶,故不設定下限,但因製造步驟之限制,0.1秒為實質下限。If the time from cooling to 500 ° C to 700 ° C is greater than 2 seconds from the end of the finishing rolling, the grain size of the old Vostian iron will become coarse. In the subsequent annealing step, the surface softening part will not be affected. Fully recrystallized. Therefore, the time from the completion of finishing rolling to cooling to 500 ° C or higher and 700 ° C or lower is set to within 2 seconds. It is preferably within 1.8 seconds, and preferably within 1.5 seconds. The shorter the time until cooling, the finer the old γ particle size becomes and it becomes easier to recrystallize, so the lower limit is not set, but 0.1 second is the substantial lower limit due to the limitation of the manufacturing steps.

只要冷卻速度滿足上述條件則不論何種速度皆可,而冷卻速度越快,越容易獲得舊γ粒徑之細粒化效果。因此,冷卻速度宜為20℃/s以上,在50℃/s以上更佳。As long as the cooling rate satisfies the above conditions, any speed may be used, and the faster the cooling rate, the easier it is to obtain the fine granulation effect of the old γ particle size. Therefore, the cooling rate is preferably 20 ° C / s or more, and more preferably 50 ° C / s or more.

若軋延後之冷卻停止溫度低於500℃,則部分之表層軟化部會成為低溫變態組織。若具有肥粒鐵與低溫變態組織之多數個組織,就會在冷軋延時不均勻地導入變形,因此不會均勻地發生再結晶,而變得容易有未再結晶組織殘存。若冷卻停止溫度為700℃以上則表層軟化部之肥粒鐵變態會延遲,因此在後續之冷軋延步驟中會無法使充分之應變蓄積於表層軟化部。故,冷卻停止溫度係設為500℃以上且700℃以下。If the cooling stop temperature after rolling is lower than 500 ° C, a part of the surface layer softened portion will become a low-temperature metamorphic structure. If there are many microstructures of ferrous iron and low-temperature metamorphic structures, deformation will be introduced unevenly during the cold rolling delay, so recrystallization will not occur uniformly, and unrecrystallized structures will easily remain. If the cooling stop temperature is 700 ° C. or higher, the deformation of the ferrite grains in the surface softening portion will be delayed. Therefore, sufficient strain cannot be accumulated in the surface softening portion in the subsequent cold rolling step. Therefore, the cooling stop temperature is set to 500 ° C or higher and 700 ° C or lower.

(冷卻至500℃以上且700℃以下之溫度後的保持時間:3秒以上) 若在500℃以上且700℃以下之溫度的保持時間小於3秒,表層軟化部之肥粒鐵便不會充分生成。較佳為保持時間在5秒以上、且以10秒以上更佳。(Holding time after cooling to a temperature of 500 ° C or higher and 700 ° C or lower: 3 seconds or more) If the holding time of a temperature of 500 ° C or higher and 700 ° C or lower is less than 3 seconds, the ferrous iron in the surface softening portion will not be sufficient generate. The holding time is preferably 5 seconds or more, and more preferably 10 seconds or more.

(捲取溫度:600℃以下) 宜在600℃以下之捲取溫度下進行捲取。藉由將捲取溫度設為600℃以下來進行捲取,低溫變態相會變得容易形成於板厚中心部,且在捲取後之冷軋步驟中對表層之應變分配量會增加,因此表層軟化部變得容易再結晶,並且變得容易使結晶粒徑更加細粒化。又,藉由將捲取溫度設為600℃以下,在捲取後之酸洗中會變得更容易去除鏽皮。而捲取溫度較佳為500℃以下,更佳為400℃以下。(Rewinding temperature: 600 ° C or lower) It should be coiled at a coiling temperature of 600 ° C or lower. When coiling is performed at a coiling temperature of 600 ° C or lower, a low-temperature abnormal phase will be easily formed at the center of the plate thickness, and the amount of strain distribution to the surface layer will increase in the cold rolling step after coiling. The surface softened portion becomes easy to recrystallize, and it becomes easy to make the crystal grain size finer. In addition, by setting the winding temperature to 600 ° C. or lower, the scale can be more easily removed during pickling after winding. The winding temperature is preferably 500 ° C or lower, and more preferably 400 ° C or lower.

為了抑制冷軋延時之斷裂,在冷卻至室溫後亦可在300℃以上且600℃以下將熱軋板回火。In order to suppress the delayed cracking of cold rolling, the hot-rolled sheet can also be tempered at a temperature above 300 ° C and below 600 ° C after cooling to room temperature.

(冷軋延之軋縮率:20%以上且70%以下) 熱軋鋼板在以常規方法施行酸洗後,會進行冷軋延。若冷軋延之軋縮率小於20%,會無法將充分之應變導入表層軟化部,而表層軟化部在後續之退火步驟中不會充分地再結晶。另一方面,若冷軋延之軋縮率大於70%則會有鋼板在軋延中斷裂的情況,因此冷軋延之軋縮率係設為20%以上且70%以下。(Cold rolling reduction: 20% or more and 70% or less) Hot-rolled steel sheets are cold-rolled after being pickled by a conventional method. If the cold rolling reduction ratio is less than 20%, sufficient strain cannot be introduced into the surface softened portion, and the surface softened portion will not be sufficiently recrystallized in the subsequent annealing step. On the other hand, if the rolling reduction rate of the cold rolling is greater than 70%, the steel sheet may be broken during rolling. Therefore, the rolling reduction rate of the cold rolling is set to be 20% or more and 70% or less.

(冷軋延後之退火熱處理:將軋延後之多層鋼板於600℃以上且750℃以下之溫度下保持5秒以上後,冷卻至室溫) 將冷軋延後之多層鋼板加熱至600℃以上且750℃以下之溫度並進行退火。若加熱保持溫度低於600℃,不但表層軟化部不會充分再結晶,且板厚中心部之雪明碳鐵也不會充分熔解,導致無法獲得穩定之殘留γ分率。若高於750℃,則會變得難以使肥粒鐵生成於板厚中心部。因此,加熱保持溫度係設為600℃以上且750℃以下。(Annealed heat treatment after cold rolling: Hold the rolled multilayer steel plate at a temperature of 600 ° C or higher and 750 ° C or lower for 5 seconds or more, and then cool to room temperature.) Heat the cold rolled multilayer steel plate to 600 ° C. Annealed at a temperature above 750 ° C. If the heating and holding temperature is lower than 600 ° C, not only the surface softened portion will not be sufficiently recrystallized, but also the cis-carbon iron in the center portion of the plate thickness will not be fully melted, resulting in that a stable residual γ fraction cannot be obtained. If it is higher than 750 ° C., it becomes difficult to generate fertilizer iron at the center of the plate thickness. Therefore, the heating and holding temperature is set to 600 ° C or higher and 750 ° C or lower.

若保持時間小於5秒,表層軟化部之未再結晶組織便不會充分再結晶。為了完全去除未再結晶組織,宜設退火時間為10秒以上,設為15秒以上更佳。而由生產性之觀點來看,宜將退火時間設為3600秒以下。If the holding time is less than 5 seconds, the non-recrystallized structure in the softened portion of the surface layer will not be sufficiently recrystallized. In order to completely remove the non-recrystallized structure, the annealing time is preferably set to 10 seconds or more, and more preferably 15 seconds or more. From the viewpoint of productivity, the annealing time should preferably be 3600 seconds or less.

為了在板厚中心部中使低溫變態組織生成,上述加熱保持後之冷卻停止溫度宜為550℃以下,較佳為300℃以下,又以100℃以下最佳。In order to generate a low-temperature metamorphic structure in the center portion of the plate thickness, the cooling stop temperature after the heating and maintaining is preferably 550 ° C or lower, preferably 300 ° C or lower, and most preferably 100 ° C or lower.

上述冷卻之後,為了低溫變態組織之軟質化及殘留沃斯田鐵之穩定化,亦可在300℃以上且550℃以下之溫度下進行回火。After the above cooling, in order to soften the low-temperature metamorphic structure and stabilize the residual Vosted iron, tempering can also be performed at a temperature of 300 ° C or higher and 550 ° C or lower.

當要對鋼板表面施行熔融鍍鋅以製造熔融鍍鋅鋼板時,係使上述在600℃以上且750℃以下之溫度下的退火後之冷卻於430~500℃的溫度範圍內停止,接著將冷軋鋼板浸漬於熔融鋅之鍍敷浴中進行熔融鍍鋅處理。鍍敷浴的條件設定在一般範圍內即可。鍍敷處理後則冷卻至室溫即可。When hot-dip galvanizing is performed on the surface of a steel sheet to manufacture a hot-dip galvanized steel sheet, the cooling after annealing at a temperature of 600 ° C to 750 ° C is stopped in a temperature range of 430 to 500 ° C, and then the cold The rolled steel sheet is immersed in a molten zinc plating bath and subjected to a hot-dip galvanizing treatment. The conditions of the plating bath may be set within a general range. After the plating process, it can be cooled to room temperature.

當要對鋼板表面施行合金化熔融鍍鋅以製造合金化熔融鍍鋅鋼板時,係在對鋼板施行熔融鍍鋅處理後,在將鋼板冷卻至室溫前於450~620℃的溫度下進行熔融鍍鋅之合金化處理。合金化處理條件設定在一般範圍內即可。When alloyed hot-dip galvanizing is performed on the surface of a steel sheet to produce an alloyed hot-dip galvanized steel sheet, the steel sheet is melted at a temperature of 450 to 620 ° C after being subjected to a hot-dip galvanizing treatment on the steel sheet before being cooled to room temperature. Galvanized alloying. The alloying treatment conditions may be set within a general range.

藉由如以上所述製造鋼板,便可製得本實施形態之鋼板。 實施例By manufacturing the steel sheet as described above, the steel sheet of this embodiment can be obtained. Examples

參照示例更具體地說明本發明鋼板。然而,以下示例為本發明鋼板之示例,本發明鋼板並不受以下示例之態樣限定。The steel sheet of the present invention will be described more specifically with reference to examples. However, the following examples are examples of the steel sheet of the present invention, and the steel sheet of the present invention is not limited to the following examples.

1.製造評估用鋼板 表2所記載之多層鋼板的製造方法為包層法之試料,係依下述方法製作而成。對具有表1所示化學組成之板厚20mm的連續鑄造鋼胚(板厚中心部用鋼板)磨削表面去除表面氧化物後,利用電弧熔接於其單面或雙面積層具有表1所示化學組成之表層用鋼板(表層軟化部)。並以表2所示之加熱溫度、熱軋延前之保持時間、精整軋延開始溫度、冷卻完成時間、冷卻停止溫度、冷卻後保持時間及捲取溫度,將所得之物進行加熱、加熱後保持、熱軋延、冷卻、冷卻後保持以及捲取成卷料,而製得積層熱軋鋼板。然後,以常規方法進行酸洗,並以表2所示之回火溫度、冷軋延率、退火溫度及退火時間進行回火、冷軋延及退火,而冷卻至室溫。1. Steel sheet for manufacturing evaluation The manufacturing method of the multi-layer steel sheet described in Table 2 is a sample of the cladding method, and was produced by the following method. After continuously grinding the surface of a 20-mm-thick continuous cast steel billet (steel plate at the center of the plate thickness) having a chemical composition shown in Table 1 to remove surface oxides, arc welding was applied to the single-sided or double-area layer. Steel sheet for chemical composition (surface softening part). The heating temperature, the holding time before hot rolling, the finishing rolling start temperature, the cooling completion time, the cooling stop temperature, the cooling holding time and the coiling temperature shown in Table 2 are used to heat and heat the obtained product. Post-holding, hot-rolling, cooling, holding after cooling, and coiling into coils to produce laminated hot-rolled steel sheets. Then, pickling was performed by a conventional method, and tempering, cold rolling, and annealing were performed at the tempering temperature, cold rolling reduction rate, annealing temperature, and annealing time shown in Table 2, and the mixture was cooled to room temperature.

表2所記載之多層鋼板的製造方法為冷噴塗法的試料,係依下述方法製作而成。The manufacturing method of the multi-layered steel sheet described in Table 2 is a sample of the cold spray method, and it was manufactured by the following method.

若為令基板為熱軋板之情況,係對具有表1所示化學組成之板厚20mm的連續鑄造鋼胚(板厚中心部用鋼板),以表2所示之加熱溫度、熱軋延前之保持時間、精整軋延開始溫度、冷卻完成時間、冷卻停止溫度、冷卻後保持時間及捲取溫度,進行加熱、加熱後保持、熱軋延、冷卻、冷卻後保持及捲取成卷料而製作出熱軋板,並在磨削表面去除表面氧化物後,於其單面或雙面利用冷噴塗法在表層形成堆積層(表層)而製作出鋼板。然後,以表2所示之回火溫度、冷軋延率、退火溫度及退火時間來進行回火、冷軋延及退火,而冷卻至室溫。For the case where the substrate is a hot-rolled sheet, a 20-mm-thick continuous cast steel slab (steel plate at the center of the sheet thickness) having a chemical composition shown in Table 1 is used. Pre-holding time, finishing rolling start temperature, cooling completion time, cooling stop temperature, holding time after cooling and coiling temperature, heating, holding after heating, hot rolling, cooling, holding after cooling and coiling into coils The hot-rolled sheet is prepared from the material, and the surface oxide is removed on the ground surface, and then a single layer or a double-sided layer is formed on the surface layer by a cold spray method to form a stacked layer (surface layer) to produce a steel plate. Then, the tempering, cold rolling, and annealing were performed at the tempering temperature, cold rolling reduction, annealing temperature, and annealing time shown in Table 2, and then cooled to room temperature.

另一方面,若為令基板為冷軋板之情況,係利用常規方法將以上述方法製作而得之熱軋板進行酸洗,並以表2所示回火溫度及冷軋延率進行回火及冷軋延而製作出冷軋板,接著利用冷噴塗法於冷軋板之至少單面形成堆積層(表層),並以表2所示退火溫度及退火時間進行退火,而冷卻至室溫。On the other hand, if the substrate is a cold-rolled sheet, the hot-rolled sheet produced by the above method is pickled by a conventional method, and is tempered at the tempering temperature and the cold rolling reduction rate shown in Table 2. Fire and cold rolling are used to produce cold-rolled sheets, and then a cold spray method is used to form a build-up layer (surface layer) on at least one side of the cold-rolled sheet, and annealing is performed at the annealing temperature and annealing time shown in Table 2 to cool to room temperature. temperature.

冷噴塗法中所使用之鐵基粒子係利用表4所示成分及粒徑之物。用於冷噴塗法之粒子,係使用依據先前技術來重複粉碎與以篩網所進行之分級而調整為預定粒子徑之物。並且,使用氮氣來作為工作氣體。利用加熱器將工作氣體加熱至700℃,且由粒子供給裝置供給鐵基粒子並混合後,以噴塗噴嘴吹附於基板而獲得多層鋼板。又,工作氣壓係固定為3MPa。並且,噴嘴之掃描速度是利用機械控制來調整。The iron-based particles used in the cold spray method are those having components and particle sizes shown in Table 4. The particles used in the cold spraying method are those which are adjusted to a predetermined particle diameter by repeatedly pulverizing and grading with a sieve according to the prior art. In addition, nitrogen is used as the working gas. The working gas is heated to 700 ° C. with a heater, iron-based particles are supplied from the particle supply device and mixed, and then the substrate is sprayed on the substrate with a spray nozzle to obtain a multilayer steel plate. The working pressure is fixed at 3 MPa. In addition, the scanning speed of the nozzle is adjusted by mechanical control.

[表1-1] [表1-2] [Table 1-1] [Table 1-2]

[表2-1] [表2-2] [table 2-1] [Table 2-2]

針對一部分之退火冷軋鋼板,在進行過最終退火後,會在460℃停止退火後之冷卻,並將冷軋鋼板浸漬於460℃之熔融鋅的鍍敷浴中2小時,而進行熔融鍍鋅處理。鍍敷浴的條件與以往相同。當不施行後述合金化處理時,在460℃之保持後,以平均冷卻速度10℃/秒冷卻至室溫。For some annealed cold-rolled steel sheets, after the final annealing, the cooling after annealing is stopped at 460 ° C, and the cold-rolled steel sheets are immersed in a molten zinc plating bath at 460 ° C for 2 hours to perform hot-dip zinc plating deal with. The conditions of the plating bath are the same as in the past. When the alloying treatment described later is not performed, after holding at 460 ° C, it is cooled to room temperature at an average cooling rate of 10 ° C / sec.

針對一部分之退火冷軋鋼板,在進行過熔融鍍鋅處理後,不冷卻至室溫而繼續施行合金化處理。加熱至520℃,並在520℃維持5秒以進行合金化處理,然後以平均冷卻速度10℃/秒冷卻至室溫。For a part of the annealed cold-rolled steel sheet, after being subjected to the hot-dip galvanizing treatment, the alloying treatment is continued without cooling to room temperature. It was heated to 520 ° C. and maintained at 520 ° C. for 5 seconds for alloying treatment, and then cooled to room temperature at an average cooling rate of 10 ° C./second.

將如上述進行而製得之退火冷軋鋼板以0.1%之延伸率進行調質軋延,而準備了各種評估用鋼板。The annealed cold-rolled steel sheet produced as described above was quenched and tempered at an elongation of 0.1%, and various steel sheets for evaluation were prepared.

2. 評估方法 對所得之退火冷軋鋼板實施:板厚測定、組織觀察、表層軟化部之氣孔率測定、維氏硬度試驗、以SEM/EBSD法進行之再結晶率測定試驗、表層軟化部之平均結晶粒徑測定、拉伸試驗、均勻延伸試驗以及V彎曲試驗。2. Evaluation method The obtained annealed cold-rolled steel sheet is subjected to: plate thickness measurement, microstructure observation, porosity measurement of surface softened part, Vickers hardness test, recrystallization rate measurement test by SEM / EBSD method, surface softened part Measurement of average crystal grain size, tensile test, uniform extension test, and V-bend test.

板厚中心部之組織的觀察方法係以如下方式進行。對鋼板表面施行鏡面研磨及膠體研磨,使板厚中心部成為測定面,並使用場發射掃描式電子顯微鏡(FE-SEM)及OIM結晶方位解析裝置,在測定面100μm平方的區域中以0.2μm間隔取得結晶方位資料群。以解析軟體(TSL OIM Analysis)解析所得之結晶方位資料群,並將組織分類。在Phase-MAP中,將被判別為沃斯田鐵相之區域判別為殘留沃斯田鐵。針對Phase-MAP中被判別為沃斯田鐵相以外之包含回火麻田散鐵、變韌鐵、保持淬火狀態的麻田散鐵以及肥粒鐵之肥粒鐵相之區域的組織,依據以3000倍的倍率觀察而得之二次電子影像更進一步地判別如下。肥粒鐵相中,在晶粒內具有下部組織者當中,於內部包含雪明碳鐵之組織係判別為回火麻田散鐵或變韌鐵。肥粒鐵相中,在晶粒內具有下部組織者當中,於內部不含雪明碳鐵之組織係判別為保持淬火狀態的麻田散。並將肥粒鐵相中,於晶粒內不含下部組織的區域判別為肥粒鐵。The method of observing the structure at the center of the plate thickness is performed as follows. The surface of the steel plate was mirror-polished and colloid-polished to make the center of the plate thickness the measurement surface. Using a field emission scanning electron microscope (FE-SEM) and an OIM crystal orientation analysis device, the measurement surface was 100 μm square and the area was 0.2 μm. The crystal orientation data group was acquired at intervals. The crystal orientation data group obtained by analysis by the analysis software (TSL OIM Analysis), and the organization was classified. In Phase-MAP, a region determined as a Vosstian iron phase is identified as a residual Vosstian iron. Regarding the organization in the Phase-MAP area that is judged to be other than the Vostian iron phase, including tempered Asada loose iron, toughened iron, Asada loose iron maintained in the quenched state, and the fertile iron phase of the fertile iron, the basis is 3000 The secondary electron image obtained by double magnification observation is further discriminated as follows. Among the ferrous grain iron phases, among those having a lower structure in the crystal grains, the structure containing Xueming carbon iron inside was judged as tempered Asada loose iron or toughened iron. Among the ferrous phase, among those having a lower structure in the crystal grains, the structure that does not contain Schiff carbon iron in the interior is judged to be as hardened as Mata San. The area of the ferrous iron phase that does not contain the lower structure in the crystal grains is identified as the ferrous iron.

以上述方法進行組織觀察,而板厚中心部之組織會被分類為肥粒鐵、回火麻田散鐵或變韌鐵、保持淬火狀態的麻田散鐵、及殘留沃斯田鐵。Observe the structure in the above method, and the structure of the central part of the plate thickness will be classified as fertile iron, tempered Asada iron or toughened iron, Asada loose iron maintained in the quenched state, and residual Vostian iron.

針對表層軟化部之組織觀察,除了使表層軟化部成為測定面以外,係以與板厚中心部之組織觀察相同的方法來進行。表層軟化部之組織實質上為肥粒鐵。The structure observation of the surface layer softened portion was performed in the same manner as the structure observation of the center portion of the plate thickness, except that the surface layer softened portion was used as the measurement surface. The structure of the surface softening part is essentially fertilized iron.

表層軟化部之氣孔率係鑑定上述研磨面的氣孔部,並利用影像處理來作為面積率而算出。表層軟化部之氣孔率,係以掃描電子顯微鏡在1000倍的倍率下進行觀察,並藉由影像處理來檢測出直徑為0.01μm以上之氣孔後,算出其合計面積率。The porosity of the surface softened portion is determined by identifying the porosity of the polished surface, and calculating the area ratio by image processing. The porosity of the softened part of the surface layer was observed with a scanning electron microscope at a magnification of 1000 times, and pores with a diameter of 0.01 μm or more were detected by image processing, and the total area ratio was calculated.

如上所述,維氏硬度試驗係為了定義表層軟化部而進行。首先,以硝太蝕劑腐蝕而使鋼板之截面組織露出,並根據由光學顯微鏡或掃描型電子顯微鏡觀察而得之組織影像,來算出鋼板之總厚度。於鋼板之板厚方向的中心,在相對於板厚方向呈垂直方向上以壓痕互不干涉之衝印間隔針對5點以壓入荷重100g重來測定維氏硬度,並以該等之平均值作為板厚方向之中心位置上的平均維氏硬度。其次,由板厚方向之中心朝向表面,將衝印間隔設為鋼板之總厚度5%的固定間隔,並在各自之板厚方向位置上與上述同樣地進行了5點之維氏硬度試驗。當某板厚方向位置上之平均維氏硬度為板厚方向之中心位置上之平均維氏硬度的0.6倍以下時,將較該位置更靠表面側定義為表層軟化部。當以5%間隔之衝印無法獲得平均維氏硬度的0.6倍以下之值而無法定義表層軟化部時,係藉由在表層之2衝印點之間,以縮得較最初衝印的間隔更短的任意固定間隔進行衝印,而定義出表層軟化部。表層軟化部用鋼板的厚度相對於板厚中心部用鋼板之板厚的比率係如表3之「表層軟化部(單側)之比率(%)」所示。As described above, the Vickers hardness test is performed in order to define the softened portion of the surface layer. First, the cross-section structure of the steel plate is exposed by the nitrate etchant, and the total thickness of the steel plate is calculated from the structure image obtained by observation with an optical microscope or a scanning electron microscope. The Vickers hardness is measured at the center of the plate thickness direction of the steel plate at a punching interval that does not interfere with each other in a direction perpendicular to the plate thickness direction. The Vickers hardness is measured at a pressure of 100 g for 5 points and the average of these is used. The value is taken as the average Vickers hardness at the center position in the thickness direction. Next, from the center of the plate thickness direction to the surface, the print interval was set to a fixed interval of 5% of the total thickness of the steel plate, and a Vickers hardness test at 5 points was performed in the same position as in the plate thickness direction. When the average Vickers hardness at a position in the thickness direction is 0.6 times or less the average Vickers hardness at the center position in the thickness direction, the surface side softer than the position is defined as the surface layer softened portion. When printing at a 5% interval cannot obtain a value less than 0.6 times the average Vickers hardness and cannot define the surface softened portion, the interval between the two printed points on the surface is used to reduce the interval from the initial printing. A shorter arbitrary fixed interval is used for printing, and the surface softening part is defined. The ratio of the thickness of the steel plate for the surface layer softened portion to the plate thickness of the steel plate for the center portion of the plate thickness is shown in "Ratio (%) of the surface layer softened portion (one side)" in Table 3.

在以SEM/EBSD法進行之再結晶率測定試驗中,對鋼板表面施行鏡面研磨及膠體研磨,使根據上述方法定義之表層軟化部的中央位置成為測定面,並使用場發射掃描式電子顯微鏡(FE-SEM)及OIM結晶方位解析裝置,在測定面100μm平方的區域中以0.2μm間隔取得了結晶方位資料群。以解析軟體(TSL OIM Analysis)解析所得之結晶方位資料群,並將第一接近測定點間之Kernel Average Misorientation(KAM值)為1.0°以下的區域定義為再結晶組織,並算出該區域之相對於總區域的面積率。In the recrystallization rate measurement test by the SEM / EBSD method, the surface of the steel plate was subjected to mirror polishing and colloidal polishing, so that the center position of the surface softening portion defined according to the above method was the measurement surface, and a field emission scanning electron microscope ( FE-SEM) and OIM crystal orientation analysis device, obtained crystal orientation data groups at intervals of 0.2 μm in a 100 μm square area of the measurement surface. An analysis software (TSL OIM Analysis) was used to analyze the crystal orientation data group, and the area where the Kernel Average Misorientation (KAM value) between the first measurement points was 1.0 ° or less was defined as the recrystallized structure, and the relative area of the area was calculated. The area ratio of the total area.

表層軟化部之平均結晶粒徑係以如下方式測定。在以SEM/EBSD法進行之平均結晶粒徑測定試驗中,利用解析軟體(TSL OIM Analysis)解析以上述方法所得之結晶方位資料群,再藉由Area Fraction法算出將具有結晶方位差15°以上之方位差的結晶晶界所包圍的區域定義為一個結晶粒時之粒徑,並算出了觀察區域整體之平均粒徑。The average crystal grain size of the surface layer softened portion was measured as follows. In the average crystal particle size measurement test by the SEM / EBSD method, the crystal orientation data group obtained by the above method was analyzed by using an analysis software (TSL OIM Analysis), and the crystal orientation difference was calculated by the Area Fraction method to be 15 ° or more. The area surrounded by the crystalline grain boundaries of the azimuth difference is defined as the particle size of one crystal grain, and the average particle size of the entire observation area is calculated.

在與鋼板之軋延方向呈直角之方向上取長軸並採取JIS5號試驗片後,測定拉伸強度(TS)及均勻延伸率(uEL)。拉伸試驗係以使用有JIS5號拉伸試驗片之JIS Z 2241所規定之方法進行。而均勻延伸試驗係以使用有平行部長度為50mm之JIS5號試驗片之JIS-Z2201所規定之方法進行。The long axis was taken in a direction perpendicular to the rolling direction of the steel sheet, and a JIS No. 5 test piece was taken, and then the tensile strength (TS) and uniform elongation (uEL) were measured. The tensile test was performed by the method prescribed by JIS Z 2241 using a JIS No. 5 tensile test piece. The uniform extension test was performed by a method prescribed in JIS-Z2201 using a JIS No. 5 test piece having a parallel portion length of 50 mm.

臨界彎曲半徑R係以使相對於軋延方向呈垂直之方向為長邊方向(彎曲稜線與軋延方向一致)來做出JIS Z2204所記載之1號試驗片後,依循JIS Z2248進行V彎曲試驗。將僅單面具表層軟化部之試樣彎曲成具表層軟化部之面成彎曲外側。衝模與衝頭之角度係設為60°並以0.1mm單位變更衝頭之前端半徑來進行彎曲試驗,而求得可不致使龜裂產生且能進行彎曲之衝頭前端半徑作為臨界彎曲半徑R。針對強度為780MPa以上且小於1180MPa之鋼種,以臨界彎曲半徑R大於1.0mm者為彎曲性不良(符號×),以1.0mm以下者為彎曲性良好(符號○),且以0.8mm以下者為彎曲性優良(◎)。針對強度為1180MPa以上之鋼種,將臨界彎曲半徑R大於2.0mm者評估為彎曲性不良(符號×),將2.0mm以下者評估為彎曲性良好(符號○),且將1.5mm以下者評估為彎曲性優良(◎)。The critical bending radius R is such that the direction perpendicular to the rolling direction is the long side direction (the bending ridge line is consistent with the rolling direction), the test piece No. 1 described in JIS Z2204 is made, and then the V bending test is performed in accordance with JIS Z2248. . Bend the sample with only the surface softened part of the single mask to the surface with the surface softened part to bend the outside. The angle between the die and the punch is set to 60 °, and the radius of the punch front end is changed by a unit of 0.1 mm to perform a bending test, and the radius of the tip of the punch capable of bending without causing cracks is determined as the critical bending radius R. For steel grades with a strength of 780 MPa or more and less than 1180 MPa, those with a critical bending radius R greater than 1.0 mm are considered to have poor bendability (symbol x), those with a strength of 1.0 mm or less are considered to have good bendability (symbol ○), and those with a strength of 0.8 mm or less Excellent bendability (◎). For steel types with a strength of 1180 MPa or more, those with a critical bending radius R greater than 2.0 mm were evaluated as poor bendability (symbol x), those with a diameter of 2.0 mm or less were evaluated as good bendability (symbol ○), and those below 1.5 mm were evaluated as Excellent bendability (◎).

對於所製得之鋼板,實際測定上述所定義之表層軟化部的板厚方向之中央位置的化學組成與板厚方向之中心位置的化學組成後,分別與表1所示表層軟化部用鋼板及母材鋼板之化學組成幾乎相同。For the obtained steel sheet, the chemical composition at the center position in the plate thickness direction and the chemical composition at the center position in the plate thickness direction of the surface softening part as defined above were actually measured, and then compared with the steel sheet for the surface softening part shown in Table 1 and The chemical composition of the base steel plate is almost the same.

平均Mn濃度係在組織截面之板厚中心部及表層軟化部各自的板厚方向中心,沿著與板厚方向呈垂直方法之線上,以50μm間隔利用EPMA測定出20點之Mn濃度,並由其平均值求出。其結果,板厚中心部之平均Mn濃度及表層軟化部之平均Mn濃度,分別與表1所示之母材鋼板及表層軟化部用鋼板之Mn濃度幾乎相同。The average Mn concentration is measured at the center of the plate thickness of the tissue cross section and at the center of the plate thickness direction of the surface softening section along the line perpendicular to the plate thickness direction. The Mn concentration at 20 points is measured by EPMA at 50 μm intervals. The average value was calculated. As a result, the average Mn concentration in the center portion of the plate thickness and the average Mn concentration in the surface layer softened portion were almost the same as those of the base material steel plate and the steel plate for the surface layer softened portion shown in Table 1, respectively.

3. 評估結果 上述評估結果顯示於表3。3. Evaluation results The above evaluation results are shown in Table 3.

[表3-1] [表3-2] [Table 3-1] [Table 3-2]

[表4] [Table 4]

表1~3中有附底線的數值係表示該數值所示之含量、條件,或表示機械特性在較佳範圍外。The underlined values in Tables 1 to 3 indicate the content, conditions, or mechanical properties outside the preferred range.

表2及表3中實施例的鋼板具有下列含Mn濃度高之鋼板的特徵,並具有優異彎曲性,前述特徵為:板厚中心部之平均Mn濃度大於4.0質量%且小於10.0質量%;表層軟化部具有鋼板之0.1%到30%的厚度,且平均Mn濃度為2.5%以下;前述表層軟化部之再結晶率為90%以上;且,具優異之TS×uEL平衡。The steel plates of the examples in Tables 2 and 3 have the following characteristics of steel plates with a high Mn concentration, and have excellent bendability. The foregoing characteristics are: the average Mn concentration at the center of the plate thickness is greater than 4.0% by mass and less than 10.0% by mass; The softened part has a thickness of 0.1% to 30% of the steel sheet, and the average Mn concentration is 2.5% or less; the recrystallization rate of the aforementioned softened part of the surface layer is 90% or more; and, it has excellent TS × uEL balance.

另一方面,表2及表3中被測材料No.2、3、6、16、18、22、24、46、49、50及52,其等之表層軟化部之再結晶率超出本發明所規定之範圍外,而未能獲得優異彎曲性。On the other hand, in the materials No. 2, 3, 6, 16, 18, 22, 24, 46, 49, 50, and 52 of Table 2 and Table 3, the recrystallization rate of the surface softening portion exceeds the present invention. Outside the specified range, excellent bendability cannot be obtained.

被測材料No.14之板厚中心部之平均Mn濃度低,而未能獲得優異之TS×uEL平衡。The average Mn concentration in the center of the plate thickness of the tested material No. 14 was low, and an excellent TS × uEL balance could not be obtained.

被測材料No.32之退火溫度高,而未能獲得優異之TS×uEL平衡。The annealing temperature of the tested material No. 32 was high, and the excellent TS × uEL balance could not be obtained.

被測材料No.33之表層軟化部之平均Mn濃度高,而未能獲得優異彎曲性。The average Mn concentration in the softened portion of the surface layer of the test material No. 33 was high, and excellent bendability was not obtained.

被測材料No.38之表層軟化部之厚度小,而未能獲得優異彎曲性。The thickness of the softened portion of the surface layer of the tested material No. 38 was small, and excellent bendability was not obtained.

被測材料No.39之表層軟化部之厚度大,而強度低。The thickness of the surface softened portion of the tested material No. 39 is large, and the strength is low.

被測材料No.46、49、50及52,其等雖是以熱軋板為基板並藉由冷噴塗法製作而成之多層鋼板,但堆積層(表層)之再結晶率低,而未能獲得優異彎曲性。The tested materials No. 46, 49, 50, and 52, although they are multilayer steel plates produced by cold-rolling with a hot-rolled plate as the substrate, have a low recrystallization rate of the stacked layer (surface layer). Can obtain excellent bendability.

被測材料No.47、48及51,其等雖是以冷軋板為基板並藉由冷噴塗法製作而成之多層鋼板,但於堆積層(表層)有氣孔產生,而未能獲得良好彎曲性。並且,表層軟化部之再結晶組織之平均結晶粒徑大,而未能獲得優異彎曲性。The tested materials Nos. 47, 48, and 51, although they are multilayer steel plates made of cold-rolled plates as substrates and produced by cold spraying methods, have pores in the build-up layer (surface layer), and have not obtained good results. Flexibility. In addition, the average crystal grain size of the recrystallized structure in the softened portion of the surface layer is large, and excellent bendability cannot be obtained.

產業上之可利用性 根據本發明,可以高生產效率來製得適合作為汽車用胚料之彎曲加工性優異且高Mn含量之高強度鋼板,而在產業上之優點多。Industrial Applicability According to the present invention, a high-strength steel sheet having excellent bending workability and a high Mn content suitable for automotive blanks can be produced with high production efficiency, and has many industrial advantages.

Claims (16)

一種高強度鋼板,包含板厚中心部、與形成於該板厚中心部之單面或雙面的表層軟化部;該高強度鋼板之特徵在於:前述板厚中心部之平均Mn濃度大於4.0質量%且小於10.0質量%,各表層軟化部具有板厚之0.1%到30%的厚度,前述表層軟化部之平均Mn濃度為2.5質量%以下,前述表層軟化部的再結晶率為90%以上,且前述表層軟化部之再結晶組織的平均結晶粒徑為0.1μm以上且40μm以下。A high-strength steel plate includes a center portion of a plate thickness and a softened portion of one or both surfaces formed at the center portion of the plate thickness. The high-strength steel plate is characterized in that the average Mn concentration in the center portion of the plate thickness is greater than 4.0 mass % And less than 10.0% by mass, each surface layer softened portion has a thickness of 0.1% to 30% of the plate thickness, the average Mn concentration of the surface layer softened portion is 2.5% by mass or less, and the surface layer softened portion has a recrystallization rate of 90% or more, The average crystal grain size of the recrystallized structure in the softened portion of the surface layer is 0.1 μm or more and 40 μm or less. 如請求項1之高強度鋼板,其中前述板厚中心部以質量%計含有:C:大於0.05%且小於0.80%、Si:0.001%以上且小於3.50%、Mn:大於4.0%且小於10.0%、P:0.10%以下、S:0.010%以下、sol.Al:0.001%以上且小於3.00%、及N:小於0.050%,且剩餘部分由鐵及無法避免之不純物所構成。For example, the high-strength steel sheet according to claim 1, wherein the center of the aforementioned plate thickness is contained in mass%: C: more than 0.05% and less than 0.80%, Si: 0.001% and more and less than 3.50%, and Mn: more than 4.0% and less than 10.0% , P: 0.10% or less, S: 0.010% or less, sol.Al: 0.001% or more and less than 3.00%, and N: less than 0.050%, and the remainder is composed of iron and unavoidable impurities. 如請求項2之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素:Cr:0.01%以上且2.00%以下、Mo:0.01%以上且2.00%以下、Cu:0.01%以上且2.00%以下、及Ni:0.01%以上且2.00%以下。The high-strength steel sheet according to claim 2, wherein the center of the aforementioned plate thickness includes at least one element selected from the group consisting of: Cr: 0.01% or more and 2.00% or less, Mo: 0.01% Above: 2.00%, Cu: 0.01% or more and 2.00%, and Ni: 0.01% or more and 2.00% or less. 如請求項2或3之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素:Ti:0.005%以上且0.30%以下、Nb:0.005%以上且0.30%以下、V:0.005%以上且0.30%以下、及W:0.005%以上且0.30%以下。The high-strength steel sheet according to claim 2 or 3, wherein the center of the aforementioned plate thickness includes at least one element selected from the group consisting of: Ti: 0.005% or more and 0.30% or less, Nb: 0.005% or more and 0.30% or less, V: 0.005% or more and 0.30% or less, and W: 0.005% or more and 0.30% or less. 如請求項2或3之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素:B:0.0001%以上且0.010%以下、Ca:0.0001%以上且0.010%以下、Mg:0.0001%以上且0.010%以下、Zr:0.0001%以上且0.010%以下、及REM:0.0001%以上且0.010%以下。The high-strength steel sheet according to claim 2 or 3, wherein the center of the aforementioned plate thickness includes at least one element selected from the group consisting of: B: 0.0001% or more and 0.010% or less, Ca: 0.0001% or more and 0.010% or less, Mg: 0.0001% or more and 0.010% or less, Zr: 0.0001% or more and 0.010% or less, and REM: 0.0001% or more and 0.010% or less. 如請求項2或3之高強度鋼板,其中前述板厚中心部以質量%計更含有選自於由以下所構成群組中之至少一種元素:Sb:0.0005%以上且0.050%以下、Sn:0.0005%以上且0.050%以下、及Bi:0.0005%以上且0.050%以下。The high-strength steel sheet according to claim 2 or 3, wherein the center of the aforementioned plate thickness includes at least one element selected from the group consisting of: Sb: 0.0005% or more and 0.050% or less, Sn: 0.0005% or more and 0.050% or less, and Bi: 0.0005% or more and 0.050% or less. 如請求項2或3之高強度鋼板,其中前述表層軟化部之C量係前述板厚中心部之C量的0.9倍以下。For example, the high-strength steel sheet of claim 2 or 3, wherein the amount of C in the softened portion of the surface layer is 0.9 times or less the amount of C in the center portion of the plate thickness. 如請求項3之高強度鋼板,其中前述表層軟化部之Cr量及Mo量的總和係前述板厚中心部之Cr量及Mo量的總和的0.9倍以下。The high-strength steel sheet according to claim 3, wherein the sum of the Cr amount and the Mo amount in the softened portion of the surface layer is 0.9 times or less the sum of the Cr amount and Mo amount in the center portion of the sheet thickness. 如請求項3之高強度鋼板,其中前述表層軟化部之Cu量及Ni量的總和係前述板厚中心部之Cu量及Ni量的總和的0.9倍以下。The high-strength steel sheet according to claim 3, wherein the sum of the amount of Cu and the amount of Ni in the softened portion of the surface layer is 0.9 times or less the sum of the amount of Cu and the amount of Ni in the center portion of the sheet thickness. 如請求項4之高強度鋼板,其中前述表層軟化部之Ti量及Nb量的總和係前述板厚中心部之Ti量及Nb量的總和的0.9倍以下。For example, the high-strength steel sheet according to claim 4, wherein the sum of the amount of Ti and the amount of Nb in the softened portion of the surface layer is 0.9 times or less the sum of the amount of Ti and the amount of Nb in the center portion of the sheet thickness. 如請求項4之高強度鋼板,其中前述表層軟化部之V量及W量的總和係前述板厚中心部之V量及W量的總和的0.9倍以下。For example, the high-strength steel sheet according to claim 4, wherein the sum of the amount of V and W in the softened portion of the surface layer is 0.9 times or less the sum of the amount of V and W in the center portion of the sheet thickness. 如請求項5之高強度鋼板,其中前述表層軟化部之B量係前述板厚中心部之B量的0.9倍以下。The high-strength steel sheet according to claim 5, wherein the amount of B in the softened portion of the surface layer is 0.9 times or less the amount of B in the center portion of the plate thickness. 如請求項1至3中任一項之高強度鋼板,其於前述表層軟化部表面更包含熔融鍍鋅層、合金化熔融鍍鋅層或電鍍鋅層。The high-strength steel sheet according to any one of claims 1 to 3, further comprising a hot-dip galvanized layer, an alloyed hot-dip galvanized layer, or an electro-galvanized layer on the surface of the aforementioned surface layer softened portion. 一種高強度鋼板之製造方法,係製造如請求項1至13中任一項之高度鋼板的方法;該高強度鋼板之製造方法之特徵在於包含以下步驟:在構成前述板厚中心部之母材鋼板的單面或雙面上積層構成前述表層軟化部之表層軟化部用鋼板,以形成多層鋼板;將前述多層鋼板加熱至1080℃以上且1300℃以下,以及在精整軋延開始溫度800℃以上且1000℃以下之條件下進行熱軋延;在前述精整軋延結束後2秒以內將前述熱軋延後之多層鋼板冷卻至500℃以上且700℃以下;在將前述多層鋼板冷卻至前述500℃以上且700℃以下之溫度後,保持3秒以上;將前述在500℃以上且700℃以下之溫度下保持3秒以上後的多層鋼板酸洗,接著以20%以上且70%以下之軋縮率進行冷軋延;及將前述冷軋延後之多層鋼板在600℃以上且750℃以下之溫度下保持5秒以上,接著進行冷卻。A method for manufacturing a high-strength steel sheet is a method for manufacturing a high-steel steel sheet according to any one of claims 1 to 13. The method for manufacturing a high-strength steel sheet is characterized in that it includes the following steps: One or both sides of the steel sheet are laminated to form the steel sheet for the surface softening part of the surface softening part to form a multilayer steel sheet; the multilayer steel sheet is heated to 1080 ° C to 1300 ° C, and the finishing rolling start temperature is 800 ° C Hot rolling is performed under the conditions above and below 1000 ° C; cooling the hot-rolled multilayer steel plate to 500 ° C or higher and 700 ° C or less within 2 seconds after the finish rolling is completed; cooling the multilayer steel plate to After the temperature of 500 ° C or more and 700 ° C or less, the temperature is maintained for 3 seconds or more; the multilayer steel plate is maintained at a temperature of 500 ° C or more and 700 ° C or less for 3 seconds or more, and then pickled at 20% or more and 70% or less Cold rolling is performed at a reduction ratio; and the multilayer steel sheet after the cold rolling is maintained at a temperature of 600 ° C. or higher and 750 ° C. or lower for 5 seconds or more, followed by cooling. 如請求項14之高強度鋼板之製造方法,其以600℃以下之捲取溫度來捲取前述在500℃以上且700℃以下之溫度下保持3秒以上後的多層鋼板。For example, the method for manufacturing a high-strength steel sheet according to claim 14 uses a coiling temperature of 600 ° C. or lower to wind the multilayer steel sheet that is maintained at a temperature of 500 ° C. or higher and 700 ° C. or lower for 3 seconds or longer. 如請求項15之高強度鋼板之製造方法,其在前述冷軋延前,在300℃以上且550℃以下之溫度下保持前述捲取後之多層鋼板並進行回火。According to the method for manufacturing a high-strength steel sheet according to claim 15, before the cold rolling, the multi-layer steel sheet after the coiling is maintained at a temperature of 300 ° C or higher and 550 ° C or lower and tempered.
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